Procrastination, stress, and self-rated health: A multi-sample meta-analysis
Despite a growing evidence base indicating that trait procrastination increases risk for specific outcomes reflecting poor health, there is less evidence examining the implications of procrastination for overall health status, or investigating the explanatory processes involved. Guided by the Cognitive Process model of self-rated health (SRH), and the Procrastination-Health model, the current study extended previous research and theory by quantifying the link between trait procrastination and SRH across multiple samples and testing the contributions of stress. Additionally, we explored the link between chronic procrastination and the SRH-FSRH discrepancy. Thirty-six samples \((N = 8,603)\) completed measures of trait procrastination, current and future SRH. A subset completed measures of perceived stress. Random effects meta-analyses were conducted on the raw and semi-partial correlations of trait procrastination with SRH and future SRH, controlling for perceived stress. Moderator analyses were conducted where warranted. Procrastination scores were examined in relation to the discrepancy between current and future SRH. Trait procrastination was significantly associated with poor SRH \((r_{avg} = .21; 95\% \; CIs \; [.19, .23])\), and to a lesser extent, poor future SRH \((r_{avg} = .13; \; 95\% CIs \; [.09, .18])\). The adjusted effects were reduced but significant for SRH, and non-significant for future SRH. Procrastination was modestly associated with a gap between current and future SRH. reflecting an expectation that health would improve slightly over the next 10 years. The current findings indicate that chronic procrastination is associated with poor overall health status that can be explained in part by higher levels of stress.
Health status, Procrastination, Self-rated health, Stress
Method
Participants and Procedure
This pre-registered study (https://osf.io/ blinded for review) analyzed data from 36 independent samples \((\text{total } N = 8603)\), including 8 undergraduate and graduate student samples and 28 community adult samples. Data were collected over a fourteen-year period (2011–2025) as part of multiple broader research programs investigating the correlates of personality and health. Ethical approval for all data collection procedures was obtained from the relevant Institutional Research Ethics Boards in the United States, Canada, and the United Kingdom.
Of the 36 data sets, all but one were collected online. In sample 4, 264 responses were collected via mail-in surveys. Except for sample 4, all samples were convenience samples recruited through the project team’s research labs. Sample 4 was recruited from a random sample of 1,000 individuals drawn from a nursing association database.
Measures
Participants provided standard demographic information, including age, gender, ethnicity, and education level (Table 1). Descriptive statistics and internal consistency estimates (Cronbach’s \(\alpha\)) for all measures are reported in Table 2.
| Age (Years) | Education Level (%) | |||||||
|---|---|---|---|---|---|---|---|---|
| Sample | N | % Female | % White | M | SD | High School | College / University | Postgraduate |
| S1 | 296 | 0.76 | 0.69 | 28.18 | 11.71 | 0.09 | 0.63 | 0.23 |
| S2 | 327 | 0.81 | 0.57 | 21.76 | 4.94 | 0.00 | 1.00 | 0.00 |
| S3 | 70 | 0.87 | 0.89 | 35.39 | 14.25 | 0.10 | 0.61 | 0.29 |
| S4 | 587 | 0.94 | 0.73 | 40.93 | 12.73 | 0.00 | 1.00 | 0.00 |
| S5 | 327 | 0.73 | 0.75 | 28.90 | 12.87 | 0.17 | 0.55 | 0.28 |
| S6 | 114 | 0.68 | 0.86 | 37.77 | 12.94 | 0.04 | 0.42 | 0.54 |
| S7 | 123 | 0.71 | --- | 20.70 | 3.16 | 0.16 | 0.83 | 0.01 |
| S8 | 101 | 0.81 | 0.65 | 32.50 | 15.40 | 0.06 | 0.73 | 0.21 |
| S9 | 318 | 1.00 | 0.81 | 24.28 | 5.38 | 0.07 | 0.59 | 0.34 |
| S10 | 318 | 0.78 | 0.81 | 28.94 | 10.80 | 0.09 | 0.53 | 0.39 |
| S11 | 150 | 0.50 | --- | 42.83 | 13.77 | 0.17 | 0.64 | 0.19 |
| S12 | 298 | 0.78 | 0.73 | 27.36 | 12.99 | 0.55 | 0.10 | 0.34 |
| S13 | 87 | 0.75 | 0.89 | 49.38 | 8.52 | 0.13 | 0.45 | 0.43 |
| S14 | 129 | 0.77 | 0.43 | 30.76 | 13.42 | 0.00 | 0.88 | 0.12 |
| S15 | 725 | 0.69 | 0.82 | 30.51 | 12.23 | 0.09 | 0.51 | 0.40 |
| S16 | 111 | 1.00 | 0.59 | 26.79 | 10.68 | 0.09 | 0.83 | 0.08 |
| S17 | 162 | 0.78 | 0.78 | 22.18 | 5.54 | 0.00 | 1.00 | 0.00 |
| S18 | 451 | 0.71 | 0.74 | 23.31 | 6.70 | 0.13 | 0.61 | 0.25 |
| S19 | 187 | 0.74 | --- | 22.50 | 5.90 | 0.00 | 1.00 | 0.00 |
| S20 | 318 | 0.77 | 0.53 | 29.26 | 13.73 | 0.00 | 1.00 | 0.00 |
| S21 | 170 | 0.74 | 0.54 | 33.48 | 17.42 | 0.12 | 0.80 | 0.08 |
| S22 | 271 | 0.70 | 0.63 | 21.32 | 4.44 | 0.00 | 1.00 | 0.00 |
| S23 | 305 | 0.76 | 0.8 | 25.56 | 12.61 | 0.21 | 0.69 | 0.10 |
| S24 | 195 | 0.82 | 0.63 | 19.86 | 2.14 | 0.32 | 0.65 | 0.03 |
| S25 | 124 | 0.76 | 0.86 | 24.35 | 11.73 | 0.34 | 0.56 | 0.10 |
| S26 | 163 | 0.69 | 0.74 | 31.09 | 13.27 | 0.15 | 0.62 | 0.24 |
| S27 | 285 | 0.69 | --- | 25.17 | 6.32 | 0.10 | 0.57 | 0.32 |
| S28 | 239 | 0.69 | --- | 30.18 | 11.83 | 0.12 | 0.67 | 0.21 |
| S29 | 266 | 0.78 | 0.56 | 20.42 | 3.74 | 0.12 | 0.87 | 0.01 |
| S30 | 322 | 0.62 | 0.8 | 36.37 | 13.95 | 0.13 | 0.60 | 0.27 |
| S31 | 346 | 0.73 | 0.74 | 28.85 | 12.78 | 0.17 | 0.55 | 0.28 |
| S32 | 106 | 0.74 | 0.45 | 24.08 | 4.51 | 0.12 | 0.28 | 0.60 |
| S33 | 132 | 0.54 | 0.81 | 21.53 | 5.33 | 0.07 | 0.93 | 0.00 |
| S34 | 100 | 0.51 | 0.66 | 24.50 | 3.49 | 0.25 | 0.56 | 0.19 |
| S35 | 100 | 0.50 | 0.97 | 65.10 | 4.53 | 0.35 | 0.41 | 0.24 |
| S36 | 280 | 0.50 | 0.78 | 39.00 | 12.30 | 0.20 | 0.56 | 0.23 |
| Trait Procrastination | Stress | Self Rated Health | Future Self Rated Health | |||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Sample (N) | α | M | (SD) | α | M | (SD) | M | (SD) | M | (SD) |
| S1 (296) | 0.9 | 2.85 | 0.67 | --- | --- | --- | 2.40 | 0.98 | --- | --- |
| S2 (327) | 0.86 | 2.68 | 0.55 | 0.84 | 2.96 | 0.55 | 2.36 | 0.85 | --- | --- |
| S3 (70) | 0.92 | 3.22 | 0.89 | 0.87 | 3.35 | 0.66 | 4.03 | 0.95 | 3.59 | 1.04 |
| S4 (587) | 0.81 | 2.87 | 0.92 | 0.86 | 2.6 | 0.58 | 2.41 | 0.86 | --- | --- |
| S5 (327) | 0.88 | 3.14 | 0.75 | 0.85 | 3.01 | 0.65 | 2.73 | 0.88 | 2.34 | 0.9 |
| S6 (114) | 0.88 | 3.41 | 0.72 | 0.88 | 2.9 | 0.67 | 2.51 | 0.83 | 2.44 | 0.83 |
| S7 (123) | 0.86 | 2.74 | 0.62 | 0.89 | 2.87 | 0.7 | 2.41 | 0.92 | 2.05 | 0.74 |
| S8 (101) | 0.89 | 2.94 | 0.81 | --- | --- | --- | 2.76 | 1.01 | 2.36 | 1.09 |
| S9 (318) | 0.9 | 3.11 | 0.79 | --- | --- | --- | 2.53 | 0.92 | 2.39 | 0.91 |
| S10 (318) | 0.9 | 3.14 | 0.83 | 0.89 | 2.99 | 0.69 | 2.79 | 0.96 | 2.43 | 0.96 |
| S11 (150) | 0.88 | 3.27 | 0.83 | 0.92 | 3.36 | 0.79 | 3.98 | 0.85 | 4.01 | 1.05 |
| S12 (298) | 0.87 | 3.06 | 0.74 | --- | --- | --- | 2.60 | 0.86 | 2.35 | 0.87 |
| S13 (87) | 0.89 | 2.83 | 0.69 | --- | --- | --- | 2.46 | 0.94 | 2.66 | 0.76 |
| S14 (129) | 0.91 | 2.93 | 0.82 | 0.88 | 3 | 0.69 | 2.67 | 0.96 | 2.57 | 0.93 |
| S15 (725) | 0.9 | 3.10 | 0.80 | --- | --- | --- | 2.40 | 0.91 | 2.4 | 0.92 |
| S16 (111) | 0.91 | 2.55 | 0.69 | --- | --- | --- | 2.80 | 0.92 | 2.55 | 1.04 |
| S17 (162) | 0.87 | 2.91 | 0.62 | 0.85 | 2.75 | 0.6 | 2.25 | 0.86 | --- | --- |
| S18 (451) | 0.9 | 3.15 | 0.77 | --- | --- | --- | 2.49 | 0.92 | 2.24 | 0.84 |
| S19 (187) | 0.88 | 2.68 | 0.58 | 0.86 | 2.92 | 0.6 | 2.20 | 0.80 | --- | --- |
| S20 (318) | 0.88 | 3.04 | 0.76 | --- | --- | --- | 2.90 | 0.83 | 2.55 | 0.84 |
| S21 (170) | 0.88 | 2.54 | 0.65 | 0.89 | 2.79 | 0.76 | 2.36 | 0.88 | --- | --- |
| S22 (271) | 0.87 | 2.70 | 0.61 | 0.87 | 2.72 | 0.68 | 2.19 | 0.79 | --- | --- |
| S23 (305) | 0.89 | 3.12 | 0.82 | --- | --- | --- | 2.26 | 0.94 | --- | --- |
| S24 (195) | 0.89 | 3.31 | 0.79 | --- | --- | --- | 2.47 | 0.90 | --- | --- |
| S25 (124) | 0.91 | 3.31 | 0.86 | --- | --- | --- | 2.29 | 0.79 | --- | --- |
| S26 (163) | 0.9 | 3.54 | 0.80 | --- | --- | --- | 2.67 | 0.96 | --- | --- |
| S27 (285) | 0.86 | 3.38 | 0.73 | --- | --- | --- | 2.48 | 0.87 | --- | --- |
| S28 (239) | 0.82 | 2.91 | 0.77 | --- | --- | --- | 2.27 | 0.95 | --- | --- |
| S29 (266) | 0.82 | 3.25 | 0.62 | --- | --- | --- | 2.32 | 0.96 | --- | --- |
| S30 (322) | 0.89 | 2.80 | 0.84 | --- | --- | --- | 2.36 | 0.91 | --- | --- |
| S31 (346) | 0.88 | 3.15 | 0.75 | --- | --- | --- | 2.74 | 0.89 | 2.36 | 0.89 |
| S32 (106) | 0.85 | 3.25 | 0.75 | --- | --- | --- | 2.44 | 0.83 | --- | --- |
| S33 (132) | 0.87 | 3.06 | 0.73 | 0.86 | 2.77 | 0.66 | 2.78 | 0.93 | 2.2 | 0.94 |
| S34 (100) | --- | 3.12 | 0.81 | --- | --- | --- | 2.57 | 1.03 | 2.46 | 0.91 |
| S35 (200) | --- | 2.80 | 0.83 | --- | --- | --- | 2.71 | 1.02 | 2.99 | 1.05 |
| S36 (280) | --- | 2.97 | 0.88 | --- | --- | --- | 2.57 | 0.98 | 2.8 | 1.05 |
Trait procrastination
Trait-level procrastination was assessed using one of three established self-report instruments: in 8 of the samples (samples 1, 2, 7, 16, 17, 19, 21, 22) the General Procrastination Scale (GPS; Lay (1986)), in 27 of the samples (samples 3, 5, 6, 8-15, 18, 20, 23-36) its 9-item short-form version (GPS-9; Sirois et al. (2019)), and in sample 4, the Revised Adult Inventory of Procrastination (AIP-R; McCown & Johnson (2001)). The GPS includes 20 items (e.g., “In preparing for some deadlines, I often waste time by doing other things”) rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree). After reverse-scoring 10 items, a mean score is calculated, with higher scores indicating a greater general tendency to procrastinate. The GPS-9 consists of 9 items (e.g., “I often find myself performing tasks that I had intended to do days before”) from the full GPS, using the response scale. Three items are reverse scored, and an average score is computed, with higher scores reflect a stronger tendency to procrastinate. The AIP-R includes 15 core items (e.g., “I often think that I don’t get things done on time”) rated on a 7-point scale from 1 (strongly disagree) to 7 (strongly agree) and 5 distractor items that are not scored. Scores are averaged, with higher scores indicate stronger procrastination tendencies
All three scales have demonstrated strong psychometric properties. Previous studies report excellent internal consistency for the GPS (\(\alpha = 0.90\); Sirois (2007)), good to excellent reliability for the GPS-9 (\(\alpha = 0.85\); Manap et al. (2023)), and similarly strong reliability for the AIP-R (\(\alpha = 0.84\); McCown & Johnson (2001)). In the present study, reliability estimates were also high: \(\text{GPS-20 } (\alpha \in [0.86 - 0.92]), \text{GPS-9 } (\alpha \in [0.81 - 0.92]), \text{and AIP-R } (\alpha = 0.81)\).
Perceived stress
In 14 of the samples (samples 2-7, 10, 11, 14, 17, 19, 21, 22, and 33) perceived stress was assessed using the Perceived Stress Scale (PSS-10; S. Cohen et al. (1983)), a 10-item measure designed to capture individuals’ appraisal of stress experienced over the past month. Participants rated each item (e.g., “In the last month, how often have you felt that you were unable to control the important things in your life?”) on a 5-point scale ranging from 0 (never) to 4 (very often). Items reflecting positive experiences or coping (e.g., “In the last month, how often have you felt confident about your ability to handle your personal problems?”) are reverse-coded, and a mean score calculated, with higher scores reflecting greater perceived stress. A prior review of the PSS-10’s psychometric properties across 12 studies reported good to excellent internal consistency (\(\alpha \in [0.74 - 0.91]\); Lee (2012)). In the current study, reliability was similarly strong, ranging from good (\(\alpha = 0.81\); sample 33) to excellent (\(\alpha = 0.91\); sample 11).
Self-rated health
Current self-rated health (SRH) was assessed with the widely used single-item measure of general health from the Medical Outcomes Survey 36 item short form (SF-36) health questionnaire (Framework, 1992). Single-item SRH measures are frequently used in health research due to their strong predictive validity for a range of outcomes (Shooshtari et al., 2007). In all samples (except sample 16), respondents rated their current health on a 5-point scale ranging from 1 (excellent) to 5 (poor). In Sample 16, a continuous measure was used ranging from 0 (poor) to 100 (excellent).
Future self-rated health (FSRH) was assessed in 20 of the samples (samples 3, 5–16, 18, 20, 31, and 33-36) using a parallel item that asked participants to anticipate the state of their physical health 10 years in the future. As with the current SRH measure, all but one sample used the same 5-point scale ranging from 1 (excellent) to 5 (poor), with sample 16, rating expectations for future health rated on the continuous 0–100 scale.
Data analysis
All data analysis was carried out using a combination of R (version 5.0; R Core Team (2025)) and SPSS (version 29.0). Pearson’s correlation coefficients were computed to examine the bivariate associations between trait procrastination and both SRH and FSRH \((r_{y1})\), between trait procrastination and perceived stress \((r_{12})\), and between perceived stress and SRH and FSRH \((r_{y2})\). Following this, to assess the unique contribution of trait procrastination to SRH and FSRH \((sr_1)\), controlling for perceived stress, semi-partial correlations were computed using the following formula:
\[sr_1 = \frac{r_{y1} \times r_{12}}{\sqrt{1 - r^2_{12}}}\]
All \(r\) values were interpreted in line with (J. Cohen, 1988) guidelines, where r = 0.10 is considered a small sized effect, r = 0.30 is considered a medium sized effect, and r = 0.50 is considered a large sized effect. The resulting adjusted correlations were subsequently included in meta-analytic models.
To estimate the average association between trait procrastination and both SRH and FSRH across studies (\(k = 36\) for SRH; \(k = 20\) for FSRH) random-effects meta-analyses were conducted using the Comprehensive Meta-analysis (CMA; Version 4) software. Prior to aggregation, CMA transforms the individual correlation coefficients \((r)\) into Fisher’s \(z\)-scores as follows: \(z = 0.5 \times ln(\frac{1+r}{1-r})\).
Heterogeneity and moderator analyses
To evaluate heterogeneity across effect sizes and determine the need for moderator analyses, two metrics were used. First, the Q statistic tested for the presence of heterogeneity across studies; a significant Q and wide confidence intervals suggested variability warranting further investigation. Second, the \(I^2\) statistic estimated the proportion of variance attributable to between-study heterogeneity rather than sampling error. Values of \(I^2 = 25\%, 50\%, \text{and } 75\%\) were interpreted as indicators of low, moderate, and high heterogeneity, respectively.
Moderator analyses were conducted to examine the potential influence of both demographic (age, percentage female) and methodological (sample type; GPS scale version) variables on the observed associations and semi-partial effects. Subgroup analyses were only conducted when there were three or more studies per subgroup, following the recommendations of Card (2015) to avoid reduced statistical power and inflated risk of spurious findings in small subgroups.
Moderator analyses followed a mixed-effects modelling approach. A random-effects model was used to analyze the combined subgroups and to estimate within-group heterogeneity. A fixed-effects model was then used to assess heterogeneity between subgroups. For continuous moderators (age, percentage female), mixed-effects meta-regressions using the method of moments were conducted. Meta-regression analyses were only performed when there were 10 or more studies in the dataset, in line with established recommendations for ensuring sufficient statistical power.
Robustness checks
The robustness of the meta-analytic findings was evaluated using Rosenthal (1979) Fail-safe \(N\), which estimates the number of unpublished or null-result studies that would be required to reduce the overall effect to non-significance. Of the 36 datasets included in the meta-analyses, 21 were unpublished. Nonetheless, the Fail-safe \(N\) was still calculated given that all datasets originated from the authors’ lab. Following Rosenthal (1979) guidelines, the Fail-safe N was considered adequate if it exceeded the threshold of \(5k + 10\), where \(k\) is the number of studies included in the analysis.
Exploratory analysis: Self-rated health discrepancy
In line with our preregistered exploratory question, we examined whether trait procrastination was associated with the discrepancy between participants current SRH and their anticipated FSRH. For each dataset, we first computed a discrepancy score by subtracting FSRH from SRH and adjusting by \(+5\) to align the scales for interpretation (Figure A1). This score reflects the relative gap between present and future health expectations, where 5 indicates no discrepancy between SRH and FSRH (SRH = FSRH), values above 5 indicate more optimistic future health ratings (SRH < FSRH) and values below 5 indicate the opposite (SRH > FSRH). Following this, we evaluated the relationship between trait procrastination and this discrepancy via a regression model fitted to each dataset. In addition, to examine whether any observed associations were accounted for by age differences, we conducted a second set of regressions that included both procrastination and age as predictors.
Finally, to synthesize effects across studies, regression coefficients (\(\beta\) values for procrastination) were extracted and subjected to random-effects meta-analysis in R using the metafor package (Viechtbauer, 2010). This was done both for the simple models (procrastination only) and the age-controlled models. The comparison of these two sets of results allowed us to evaluate whether the observed links between procrastination and the SRH-FSRH discrepancy remained after adjusting for age, or whether they were largely explained by the age-relayed variance.
Results
Of the 36 datasets, 28 contained missing values on key variables and were assessed for patterns of missingness using Little (1988) MCAR test from the naniar package (Tierney & Cook, 2023). Following the recommendations of (Jakobsen et al., 2017), datasets with a non-significant MCAR test \((k = 18)\) were imputed using linear interpolation from the zoo package (Zeileis & Grothendieck, 2005). For datasets where the MCAR test was significant \((k = 10)\), missing values were addressed using multiple imputation with chained equations from the mice package (van Buuren & Groothuis-Oudshoorn, 2011).
Trait procrastination and SRH
A meta-analysis of unadjusted correlations across the 36 samples \((\text{total } N = 8603)\) revealed a significant, positive, medium-sized association between procrastination and SRH (see Table 3). Tests of heterogeneity indicated no significant unexplained variability among effect sizes \(Q(35) = 43.53, p = 0.155, I^2 = 19.45\%\), indicating that moderator analyses were not warranted.
Trait procrastination, perceived stress, and SRH
The meta-analysis of associations between procrastination and perceived stress across 14 samples revealed the expected positive relationship (see Table 3). Heterogeneity tests indicated moderate variability among effect sizes, \(Q(13) = 27.21, p = 0.012, I^2 =52.22\%\). For perceived stress and SRH, consistent positive associations were observed across the same 14 samples, with an overall medium-sized effect (see Table 3). Heterogeneity was non-significant, \(Q(13) = 17.60, p = 0.173, I^2 =26.14\%\), and moderator analyses were therefore omitted.
A meta-analysis of semi-partial correlations (adjusted for perceived stress) revealed a small but significant positive association between procrastination and SRH (see Table 3). Similar to the unadjusted analyses, there was no evidence of heterogeneity, \(Q(13) = 12.99, p = 0.449, I^2 =0\%\). Compared to the medium-sized unadjusted effects, the adjusted effects were reduced in magnitude, suggesting that perceived stress partially accounted for the procrastination - SRH association.
| Sample | N | Type | Measure | PRO-SRH (r) | PRO-Stress (r) | Stress-SRH (r) | PRO-SRH (Sr) |
|---|---|---|---|---|---|---|---|
| <em>Note.</em> AIPR = Revised Adult Inventory of Procrastination (McCown et al., 1989); GPS 20 = General procrastination scale (Lay, 1986); GPS-9 = 9-item GPS (Sirois et al., 2019). S = Student, C = Community. | |||||||
| S1 | 296 | C | GPS 20 | 0.28 | --- | --- | --- |
| S2 | 327 | S | GPS 20 | 0.25 | 0.31 | 0.29 | 0.18 |
| S3 | 70 | C | GPS 9 | 0.22 | 0.60 | 0.32 | 0.04 |
| S4 | 587 | C | AIPR | 0.22 | 0.40 | 0.33 | 0.10 |
| S5 | 327 | C | GPS 9 | 0.23 | 0.40 | 0.32 | 0.12 |
| S6 | 114 | C | GPS 9 | 0.10 | 0.40 | 0.43 | -0.08 |
| S7 | 123 | S | GPS 20 | 0.36 | 0.57 | 0.32 | 0.23 |
| S8 | 101 | C | GPS 9 | 0.10 | --- | --- | --- |
| S9 | 318 | C | GPS 9 | 0.20 | --- | --- | --- |
| S10 | 318 | C | GPS 9 | 0.21 | 0.42 | 0.40 | 0.05 |
| S11 | 150 | C | GPS 9 | 0.22 | 0.41 | 0.45 | 0.05 |
| S12 | 298 | C | GPS 9 | 0.20 | --- | --- | --- |
| S13 | 87 | C | GPS 9 | 0.02 | --- | --- | --- |
| S14 | 129 | C | GPS 9 | 0.15 | 0.29 | 0.29 | 0.07 |
| S15 | 725 | C | GPS 9 | 0.18 | --- | --- | --- |
| S16 | 111 | C | GPS 20 | 0.10 | --- | --- | --- |
| S17 | 162 | S | GPS 20 | 0.06 | 0.24 | 0.12 | 0.03 |
| S18 | 451 | S | GPS 9 | 0.26 | --- | --- | --- |
| S19 | 187 | S | GPS 20 | 0.18 | 0.35 | 0.29 | 0.09 |
| S20 | 318 | C | GPS 9 | 0.29 | --- | --- | --- |
| S21 | 170 | C | GPS 20 | 0.10 | 0.32 | 0.39 | -0.03 |
| S22 | 271 | S | GPS 20 | 0.18 | 0.27 | 0.37 | 0.09 |
| S23 | 305 | C | GPS 9 | 0.23 | --- | --- | --- |
| S24 | 195 | S | GPS 9 | 0.26 | --- | --- | --- |
| S25 | 124 | C | GPS 9 | 0.24 | --- | --- | --- |
| S26 | 163 | C | GPS 9 | 0.14 | --- | --- | --- |
| S27 | 285 | C | GPS 9 | 0.11 | --- | --- | --- |
| S28 | 239 | C | GPS 9 | 0.26 | --- | --- | --- |
| S29 | 266 | C | GPS 9 | 0.18 | --- | --- | --- |
| S30 | 322 | C | GPS 9 | 0.14 | --- | --- | --- |
| S31 | 346 | C | GPS 9 | 0.23 | --- | --- | --- |
| S32 | 106 | C | GPS 9 | 0.16 | --- | --- | --- |
| S33 | 132 | S | GPS 9 | 0.15 | 0.42 | 0.27 | 0.04 |
| S34 | 100 | C | GPS 9 | 0.40 | --- | --- | --- |
| S35 | 100 | C | GPS 9 | 0.23 | --- | --- | --- |
| S36 | 280 | C | GPS 9 | 0.37 | --- | --- | --- |
| Average r (k) | 0.21 | 0.38 | 0.33 | 0.08 | |||
| 95% CI | [0.91-0.23] | [0.33-0.43] | [0.29-0.37] | [0.05-0.12] | |||
| N | 8,603 | 3,067 | 3,067 | 3,067 | |||
Trait procrastination and FSRH
A meta-analysis of unadjusted correlations across the 20 samples \((\text{total } N = 4598)\) revealed a significant, positive, small-sized association between procrastination and FSRH (see Table 4). Tests of heterogeneity indicated there was significant unexplained variability among effect sizes \(Q(19) = 37.55, p = 0.007, I^2 = 49.41%\), suggesting that moderator analyses were warranted.
Moderator analyses for the possible impact of GPS scale version and sample type could not be conducted as there were fewer than 3 studies per subgroup for each of these analyses. The meta-regression testing the potential influence of participant age on the unadjusted effects for trait procrastination and FSRH was non-significant, \(\beta = -0.00 [.00, -.01], Q_{model}(1) = 0.01, p = .90, Q_{residual}(18) = 37.55, p = .004\). However, the meta-regression examining the influence of participant sex on the associations of trait procrastination with SRH were significant, \(\beta = -0.36 [-.65, -.08], Q_{model}(1) = 6.32, p = .01, Q_{residual}(18) = 28.41, p = .06, \text{analog } R^2 = .41\). This indicated that as the proportion of females in the sample increased, the magnitude of the associations between trait procrastination and poor FSRH decreased.
Trait procrastination, perceived stress, and FSRH
The meta-analysis of associations between procrastination and perceived stress across 8 samples revealed the expected positive relationship (see Table 4). Heterogeneity tests indicated no variability among effect sizes, \(Q(7) = 11.79, p = 0.108, I^2 = 40.62\%\). For perceived stress and SRH, consistent positive associations were observed across the same 14 samples, with an overall small to medium-sized effect (see Table 4). Again, heterogeneity was non-significant, \(Q(7) = 14.01, p = 0.051, I^2 = 50.04\%\).
Lastly, a meta-analysis of the semi-partial correlations (adjusted for perceived stress) revealed a small but non-significant positive association between procrastination and FSRH (see Table 4). Similar to the unadjusted analyses, there was no evidence of heterogeneity, \(Q(7) = 3.80,p = 0.802, I^2 =0\%\).
| Sample | N | Type | Measure | PRO-FSRH (r) | PRO-Stress (r) | Stress-FSRH (r) | PRO-FSRH (Sr) |
|---|---|---|---|---|---|---|---|
| <em>Note.</em> GPS 20 = General procrastination scale (Lay, 1986); GPS-9 = 9-item GPS (Sirois et al., 2019). S = Student, C = Community. | |||||||
| S3 | 70 | C | GPS 9 | 0.30 | 0.60 | 0.46 | 0.03 |
| S5 | 327 | C | GPS 9 | 0.10 | 0.40 | 0.16 | 0.04 |
| S6 | 114 | C | GPS 9 | 0.12 | 0.40 | 0.35 | -0.02 |
| S7 | 123 | S | GPS 20 | 0.15 | 0.57 | 0.13 | 0.10 |
| S8 | 101 | C | GPS 9 | 0.01 | --- | --- | --- |
| S9 | 318 | C | GPS 9 | 0.10 | --- | --- | --- |
| S10 | 318 | C | GPS 9 | 0.05 | 0.42 | 0.23 | -0.05 |
| S11 | 150 | C | GPS 9 | 0.19 | 0.41 | 0.32 | 0.07 |
| S12 | 298 | C | GPS 9 | 0.12 | --- | --- | --- |
| S13 | 87 | C | GPS 9 | -0.22 | --- | --- | --- |
| S14 | 129 | C | GPS 9 | 0.10 | 0.29 | 0.08 | 0.08 |
| S15 | 725 | C | GPS 9 | 0.09 | --- | --- | --- |
| S16 | 111 | C | GPS 20 | 0.09 | --- | --- | --- |
| S18 | 451 | S | GPS 9 | 0.21 | --- | --- | --- |
| S20 | 318 | C | GPS 9 | 0.11 | --- | --- | --- |
| S31 | 346 | C | GPS 9 | 0.10 | --- | --- | --- |
| S33 | 132 | S | GPS 9 | 0.15 | 0.42 | 0.19 | 0.08 |
| S34 | 100 | C | GPS 9 | 0.38 | --- | --- | --- |
| S35 | 100 | C | GPS 9 | 0.24 | --- | --- | --- |
| S36 | 280 | C | GPS 9 | 0.28 | --- | --- | --- |
| Average r (k) | 0.13 | 0.43 | 0.22 | 0.03 | |||
| 95% CI | [.09, .18] | [.37, .49] | [.167, .27] | [-.02, .08] | |||
| N | 4,598 | 1,363 | 1,363 | 1,363 | |||
Procrastination and discrepancy between SRH and FSRH
An exploratory analysis of discrepancy between current and future SRH across 20 of the 36 samples (mean discrepency \(\in [4.33-5.58]\); Figure A1) revealed that the association with trait procrastination was inconsistent across samples. In 9 of the samples (samples 5, 7, 9, 10, 13, 15, 18, 20, and 31), higher procrastination scores were significantly associated with a larger gap between current and future SRH, with small-to-moderately sized beta values \((\beta \in [0.09-0.35])\). These results suggest that in some samples, individuals with higher levels of procrastination tended to anticipate greater improvements in their future health relative to their current health. However, several studies showed no reliable effect, with some showing non-significant negative effects (e.g., sample 3: \(\beta = -0.11, p = 0.322\)), and others having non-significant positive effects (e.g., sample 34: \(\beta = 0.07,p = 0.425\)). This pattern indicates there is substantial variability in the observed associations across independent samples.
To synthesise these findings and test whether this variability was significant, we conducted a random effects meta-analysis pooling the 20 available samples (Figure 3). The overall effect was small but statistically significant \((β_pooled = 0.10 [0.07-0.13]; p< 0.001)\), with no evidence of between-study heterogeneity \((Q(19) = 24.50, p = 0.179, I^2 = 13.0\%)\). Taken together, these exploratory findings provide preliminary evidence that trait procrastination may sometimes be linked to overly optimistic expectations about future health, although the effect is modest in size.
In addition to the simple regression models, we conducted a second set of analyses controlling for age to assess whether the association between trait procrastination and the SRH-FSRH discrepancy was independent of age-related differences. Across the 20 samples, the inclusion of age as a covariate attenuated some of the previously observed effects, although several significant associations remained. In 5 of the samples (samples 7, 10, 13, 18, and 20) higher procrastination scores were significantly associated with a larger gap between current and future SRH, with small-to-moderately sized beta values \((\beta \in [0.09 - 0.34\).
Again, to synthesise these adjusted effects, we pooled the regression coefficients for procrastination (controlling for age) using a random effects meta-analysis for the 20 available samples (Figure A2). The overall adjusted effect was smaller in size but remained statistically significant \((β_pooled = 0.07 [0.04-0.10]; p<0.001)\). Consistent with the unadjusted models, there was no evidence of between-study heterogeneity \((Q(19) = 23.06, p = 0.235, I^2 = 0.1\%)\).
Robustness checks
The Failsafe \(N\) analysis for the unadjusted correlations between trait procrastination and SRH found that to reduce the p value below \(.05\) and render the average effect non-significant, an additional \(3262\) studies with non-significant results would need to be included in the set of studies that were statistically meta-analysed. This value was well above the 5k + 10 studies cutoff (190) recommended by Rosenthal (1979).
Because one sample used a measure of trait procrastination that was not a version of the GPS, a sensitivity analysis was conducted for the effects in the overall meta-analysis of the unadjusted effects. When Sample 4, which used the AIPR, was removed, the overall average effect remained the same, \(r_{avg} = 0.21, 95\% CI [.19 - .23], Q(34) = 43.40, p = 0.129, I^2 = 21.66%\), indicating that this variation in procrastination measurement did not significantly impact the overall magnitude of the average association between procrastination and SRH.
Discussion
The current study replicated and extended previous research and theory by quantifying the link between trait procrastination and poor SRH through a robust analysis of 36 diverse samples. Crucially, we also applied the cognitive process model of SRH and the procrastination-health model to test the potential contribution of stress to the procrastination-SRH link and provide insights into the potential processes involved. Across all samples, procrastination was associated with poor SRH, with a small to moderate but significant average association, and a non-significant degree of variability. Consistent with our hypothesis and both models, when the contributions of perceived stress were accounted for, the magnitude of this association was noticeably attenuated, but remained significant. Lastly, the analysis of a subset of 20 samples found that procrastination was significantly associated with poor future SRH, although the average association was small in magnitude. These associations were found to vary significantly, with the magnitude of the associations increasing as the proportion of males in the sample increased. Similar to the analysis of the adjusted associations between procrastination and SRH, when stress was accounted for the magnitude of the average association decreased and was no longer significant.
The current findings contribute to and extend a growing evidence base that underscores the negative health consequences of chronic procrastination in several important ways. Previous research on the risks of procrastination for health have tended to focus on specific aspects of health, including health behaviours, sleep, stress, physical symptoms, and illness (Johansson et al., 2023; Kelly & Walton, 2021; Li et al., 2020; Sirois, 2015; Sirois et al., 2015, 2023) rather than overall health. Using SRH as a summary measure of health status, we found evidence that procrastination is also linked to poor overall health, and not just specific aspects. This makes sense if we consider that SRH is a robust summary measure of objective health indicators and outcomes (Jylhä, 2009), including key biomarkers for health (Kananen et al., 2021). Although previous research linking procrastination to SRH is scant and inconclusive, the results of our analysis of 36 samples provides a clearer picture of how and why chronic procrastination is linked to poor SRH. Our analyses also suggest that the link between chronic procrastination and SRH is relatively consistent across university student and adult samples, and is unaffected by demographic factors.
Another noteworthy contribution of the current research is the application of two models to understand not just how procrastination is linked to poor SRH, but also why. Consistent with both the Cognitive Process model (Jylhä, 2009) and the Procrastination-Health model (Sirois et al., 2003; Sirois, 2007), we found evidence that higher perceived stress explains in part why procrastination is associated with poor SRH. This finding suggest that both models provide plausible and complimentary explanations for why procrastination may be associated with poor SRH. However, in the absence of significant heterogeneity and therefore moderation via the demographic factors suggested by the Cognitive Process model, the Procrastination-Health model may provide a more parsimonious explanation for why chronic procrastination contributes to poor SRH. Nonetheless, the consistency of our findings with both models suggests that the psychophysiological processes involved in repeated stress experiences linked to procrastinating, alongside the influence of stress on the cognitive processes involved in evaluating health states, provide reasonable explanations for the health risks associated with chronic procrastination.
The current study also provided a novel test of the implications of chronic procrastination for expectations for future health states by testing a temporal variant of SRH, future SRH. Although the findings generally paralleled those for current SRH, there were several noteworthy differences. The magnitude of the average association with chronic procrastination was smaller for FSRH, and when adjusted for stress, the pooled association was no longer significant. There was also a significant degree of heterogeneity in the unadjusted effects that was due in part to participant sex, with the association between procrastination and poor FSRH becoming stronger for samples with a greater proportion of males. From the lens of the Cognitive process model (Jylhä, 2009), biological sex is one personal-historical factor that can shape evaluations of health in multiple ways, including through awareness of the gender gap in life expectancy, which favours women (Rochelle et al., 2015). Additionally, chronic procrastination is known to be more prevalent amongst males compared to females (Lu et al., 2022). Taken together, these and other factors may result in male procrastinators having more negative expectations for their future health states.
The exploratory analysis of how trait procrastination might be implicated in the gap between evaluations of current and future SRH revealed interesting findings that highlight the role of biases in expectations for future health. Although procrastination was associated overall with lower future SRH, the small but significant pooled association with the discrepancy with future SRH indicates that for some samples, people prone to procrastination expected that their health in 10 years would be better than it was currently, even after controlling for age differences. This finding may seem counterintuitive given that procrastination was overall associated with expectations for poor health in the future. However, it is important to consider that this discrepancy analysis is relative to current health states. For example, current health may be viewed as poor by someone who chronically procrastinates; yet they may believe that it will still be poor 10 years in the future but to a lesser degree than it is currently. Nonetheless, this expectation runs counter to what we know about the decline of health states in general over time, especially as a result of aging (Jylhä, 2009). Accordingly, this optimistic bias towards future health amongst people who chronically procrastinate may be a reflection of wishful thinking (Sigall et al., 2000), and or a general tendency to use avoidant coping to deal with unpleasant realisations (Sirois & Kitner, 2015). Thus, people prone to procrastination may avoid giving full considerations to their current poor health habits and states when appraising their future health. Alternatively, apparent optimistic views of health improving in the next 10 years may be fueled in part by the difficulties in future-oriented thinking associated with chronic procrastination (Blouin-Hudon et al., 2016; Blouin-Hudon & Pychyl, 2017; Sirois, 2014). Although this discrepancy was not very large, and for several samples there was no significant gap between current and future SRH, further research testing these competing explanations would be useful to provide more definitive insights into this unusual finding.
Limitations and strengths
Though novel, the current findings should be considered in the context of several limitations. The current analyses relied upon data garnered from cross-sectional studies, making it difficult to confirm the proposed directionality of the associations which assumes the temporal precedence of trait procrastination in relation to SRH. Indeed, trait procrastination when measured by the GPS (Lay, 1986) has demonstrated excellent temporal stability over a 10 year period (Steel, 2007), and is considered a moderately heritable trait (Gustavson et al., 2014). Together, this evidence and the framework of the cognitive process model (Jylhä, 2009) provide support for expecting that procrastination influences SRH, rather than the reverse.
Because procrastination can be both a cause and consequences of stress (Johansson et al., 2023; Sirois, 2023; Sirois et al., 2023), determining the directionality of the links between procrastination and stress as suggested by the procrastination-health model is less straightforward and cannot be established by the current analyses. We acknowledged this by focusing instead on the contributions of stress to explaining why trait procrastination might be linked to poor SRH. Consequently, further research examining the potentially dynamic, reciprocal, and likely mutually reinforcing linkages between procrastination and stress and their influence on evaluations of health is needed to confirm the predominant directionality.
The strengths of the current research include testing our research hypotheses across large sets of independent and diverse samples, with the overall statistical meta-analysis of procrastination and SRH conducted across 36 samples totaling 8,603 participants. This MOD analytic approach provided not only support for the generalisablity of the findings across student and non-student samples, but also the opportunity to conduct robust tests of how and why procrastination is linked to SRH to build a strong evidence base for an understudied area (Cumming, 2014). This would not have been possible with a traditional meta-analysis framework which requires having a sufficient evidence base to analyse.
Conclusions
This analysis of 36 samples provides robust evidence that chronic procrastination is associated with poor self-rated current and to a lesser extent, future self-rated health. Consistent with the Cognitive Process model (Jylhä, 2009) and the Procrastination-health model (Sirois et al., 2003; Sirois, 2007), we found evidence that high levels of perceived stress explains in part why people prone to procrastination report poorer overall health. Exploratory analyses suggest that some people prone to procrastination may hold unrealistically optimistic expectations about their future health, which could undermine motivation to adopt healthier behaviours. Taken together, these findings underscore the importance of considering chronic procrastination not only as self-regulatory failure with academic or occupational costs, but also as a behaviour pattern with significant and negative implications for overall health status.