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Impact of Sources of Strength on adolescent suicide deaths across three randomized trials
  1. Peter Wyman1,
  2. Ian Cero1,
  3. Charles Hendricks Brown2,
  4. Dorothy Espelage3,
  5. Anthony Pisani1,
  6. Tomei Kuehl4,
  7. Karen Schmeelk-Cone1
  1. 1 Psychiatry, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA
  2. 2 Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA
  3. 3 Education, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
  4. 4 Consulting Within Your Context LLC, Denver, Colorado, USA
  1. Correspondence to Dr Peter Wyman, Psychiatry, University of Rochester School of Medicine and Dentistry, Rochester, New York, 14642, USA; peter_wyman{at}


Universal interventions are key to reducing youth suicide rates, yet no universal intervention has demonstrated reduction in suicide mortality through an RCT. This study pooled three cluster-RCTs of Sources of Strength (n=78 high schools), a universal social network-informed intervention. In each trial, matched pairs of schools were assigned to immediate intervention or wait-list. Six schools were assigned without a pair due to logistical constraints. During the study period, no suicides occurred in intervention schools vs four in control schools, that is, suicide rates of 0 vs. 20.86/100,000, respectively. Results varied across statistical tests of impact. A state-level exact test pooling all available schools showed fewer suicides in intervention vs. control schools (p=0.047); whereas a stricter test involving only schools with a randomised pair found no difference (p=0.150). Results suggest that identifying mortality-reducing interventions will require commitment to new public-health designs optimised for population-level interventions, including adaptive roll-out trials.

  • Adolescent
  • Suicide/Self?Harm
  • Program evaluation
  • Mortality
  • School

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  • No universal suicide prevention programme has previously demonstrated reduction in youth suicide deaths through an RCT.


  • Analysis combining three cluster randomised trials (n=78 schools) suggested that the Sources of Strength programme may reduce suicide mortality in schools.

  • Results varied across statistical models, with the intervention condition showing a reduction in suicides in a state-level test including all schools versus no significant reduction in a test involving only schools with a randomised pair.


  • Sources of Strength and other network-based interventions are a uniquely promising strategy for reducing youth suicide mortality and worthy of broader population roll-out studies.

  • Larger state-wide roll-out trials are needed to confirm these promising results.

Youth suicide is a leading cause of death and years of life lost world wide.1 In the United States in 2020, for example, suicide was the second leading cause of death for people ages 10–14 and third leading cause for ages 15–24.2

Universal interventions targeting broad youth populations are likely essential to achieve significant population reductions in suicide rates for at least two reasons.3 4 First, strategies limited to already identified high-risk individuals will not capture most youth who will die by suicide, the majority of whom are not seen by a mental health professional in the months prior to death.5 A second reason is the limited availability and accessibility to effective clinical services for many populations with high suicide rates (eg, Indigenous, rural and other underserved communities). Despite emerging consensus on the need for population strategies, no universal intervention has yet demonstrated a reduction in youth suicide mortality through a randomised controlled trial (RCT).

Among the class of universal interventions, those that strengthen relationship structures and social norms around youth and emerging adults are uniquely promising for suicide prevention.6 7 For youth who are already at elevated risk or suicidal, natural social networks are often the only pathway to formal clinical services (ie, based on their status as minors, they typically cannot navigate these systems independently and require supportive encouragement).8 For youth who are currently healthy (but a portion of whom will become suicidal), stronger social integration and healthy peer norms can prevent future vulnerability to becoming suicidal.6 7 Taken together, social network interventions thus build proactive suicide protection into the social environment,9 10 and address both the multifaceted drivers of youth suicide and extended time scales in which suicide can emerge.

Sources of Strength is a social network-informed intervention that trains diverse youth key opinion leaders to disseminate a multidimensional coping framework through their friendship groups by conducting school-wide prevention campaigns. The objective is reducing suicide risk across a school’s full school student population. Three cluster (school) RCTs have been conducted. In an initial efficacy trial testing target engagement of programme mediators, Sources of Strength improved school-wide protective norms (eg, help seeking acceptability) and student help-seeking behaviours (eg, referral of suicidal friends to adults).11 A second hybrid effectiveness-implementation trial showed Sources of Strength increased student help-seeking behaviours over one school year that were subsequently lost when implementation fidelity declined, and no overall beneficial effects on student suicide attempts.12 A third trial that tested for cross-over effects on sexual violence13 showed significant reductions in suicide attempt rates (student self-report) over a 2 year school period.14

Taken together, prior findings suggest at least the potential for this social network intervention to reduce adolescent suicide mortality. However, no prior trial examined Sources of Strength impact on student suicide mortality. To evaluate its effectiveness for reducing suicide fatalities, this investigation pooled these three group-randomised controlled trials spanning 78 high schools.


In each of these RCTs, high schools were stratified (location, size, timing) to form matched pairs and randomly assigned to either immediate Sources of Strength (intervention) or to the wait-list condition. Six schools were assigned without a pair due to logistical constraints. In the first trial,11 intervention schools implemented Sources of Strength for one school semester and control schools began implementing in the second semester (see table 1). In the second12 and third trials,13 intervention schools implemented the programme for two school years, with control schools starting in year three.

Table 1

Trials of Sources of Strength, suicide deaths and rates per 100 000 student years

Counts of suicide deaths across all trials came from mandatory school reports to the Data Safety Monitoring Committees/IRBs detailing any suicides among each school’s student population during the study period when intervention schools were implementing and control schools had not yet started. This active study period for counting suicide deaths ended once control schools began implementing Sources of Strength, since any deaths after that point could not be attributed to difference in intervention exposure across the two randomised conditions.

To determine if the suicide rate differed by randomised condition across the three aggregated trials, student years of exposure to condition (intervention or control) was calculated. For each school, this was calculated as the total student population X duration of the exposure period. The exposure start-date was date of training for student peer leaders in the intervention condition (same start-date in matched control school). The exposure period lasted through first semester in trial #1 and end of the second school year in trials #2 and #3. Condition was based on a school’s assigned condition (ITT). Because suicide deaths are relatively rare occurrences, an exact conditional test of a common OR of 1 between condition and suicide was used to determine if the association between suicide rates and condition was non-random. We conducted two exact tests: (a) one including all 78 schools (trial X state=6 strata), and (b) the other with only the matched pairs of 72 schools (36 pairs=36 strata). The first model is thus a state-level analysis and also includes more schools; whereas the second includes a smaller sample, but is a stricter statistical control for baseline characteristics.


The three cluster RCTs with 78 schools accounted for 40 747 student years of exposure: 21 576 to intervention and 19 172 to control conditions. Across all three trials, no suicides occurred in the intervention schools (point estimate of 0). Four suicides occurred in control schools that had not yet implemented Sources of Strength, representing an aggregated suicide rate of 20.86 per 100 000 person years (table 1).

The first exact test that pooled the 78 schools by state and trial showed the suicide event rate was lower in intervention compared with control schools (p=0.047). In the second test comparing the 72 schools randomised in pairs, no significant difference was observed (p=0.150).


Sources of Strength is a universal school-based social network intervention with a growing evidence base. To extend knowledge about this intervention, this study examined impact on student suicide mortality. This study’s results combining three prior trials (n=78 high schools) suggest Sources of Strength reduced student suicides, but also that broader state-wide roll out trials are needed to confirm this initially promising signal. Specifically, if the current results are replicated, scaling up the programme across a moderate-sized state could translate to more than 100 saved lives over a decade. However, this study also underscores limitations of traditional RCT designs – that enroll and follow individual people – to identify population level suicide impacts, even when combining multiple large trials as in this study. Identifying mortality-reducing interventions instead demands commitment to new public-health designs.

We specifically recommend “adaptive roll out” trials that sequentially randomise blocks of communities or regions in a state to receive an intervention such as Sources of Strength at different phases.15 Such an approach can leverage ongoing surveillance of suicides in a larger number of new intervention sites (ie, not requiring new data collection for deaths), dramatically increasing power to detect impact on mortality. In addition to sequential roll-out and comparison of sites randomised to different implementation timing, these trial designs build in the expectation of an iterative implementation refinement based on what is learnt in early cohorts, along with systematic tracking of implementation practices.

The observed modifications to Sources of Strength over 15 years in which these three trials were conducted demonstrates this point regarding refinement in implementation over time. Trial one was focused on efficacy for target engagement of key intervention mediators, although suicide deaths were also collected as part of the safety monitoring in this trial. During this initial phase Sources of Strength focused on training student peer leaders. With that sole focus, Sources of Strength was then tested in an implementation-effectiveness hybrid trial (trial 2), which showed short term benefits on targeted mediators (ie, more students school-wide engaged adults for support) and findings supported an indirect effect of increased adult support in the first school year on reduced suicide attempts; however, those benefits were lost in the second school year as implementation fidelity waned, and Sources of Strength showed no overall benefit on reduced suicide attempts by the end of the second school year and became potentially iatrogenic for ninth grade students when implemented in schools with low fidelity (ie, non-adherence to recommended peer-led messaging campaigns).12 In a more recent trial (trial 3) testing Sources of Strength after significant expansion in training and implementation resources provided to adults who mentor student peer leaders, the programme showed more consistent, beneficial effects on reducing suicidal behaviours.14

This study has several strengths. A key strength is this study evaluated intervention efficacy for an outcome of high public health significance that is seldom possible to evaluate in a clinical trials framework. Suicide deaths among high school students are a major source of years of life lost both in the US and worldwide1 and few interventions have been shown under conditions of randomization to reduce it. Second, the very same outcome measure was used across the three trials in the same age-group, unlike many other RCT synthesis analyses that combine heterogenous measures and population groups.16 And across these three trials, suicide deaths were collected in the same manner. However, although there were these key areas of standardisation across trials (measure, population), this study is still affected by known variability in implementation – a common methodological challenge in trial synthesis studies. Third, these trials strategically sampled a large diverse cross-section of high school students from a range of socioeconomic backgrounds and social contexts (eg, urban and rural, ethnicity, geographic region, school size).

This study also has some limitations. First is the variability across trials in the duration of the active trial period during which deaths were tracked (ie, trial one was one school semester vs two school years in trials 2 and 3). Because there were no student suicide deaths in trial 1, no adjustments were made to account for variability in study duration across trials. Moreover, with only three trials it is difficult to meaningfully disentangle the effect of trial length on suicide deaths. A second limitation is that, although the base rate of suicide mortality across these trials was comparable to the general youth population in the U.S., the outcome is still sufficiently rare that it may have suppressed statistical power for one or both models tested. Simply put, an exact test with a low number of events has low statistical power. A third and possibly related limitation is that study results were variable across statistical tests. Specifically, the test with the smaller number of paired schools (stricter control for baseline differences) did not detect an intervention effect on mortality, whereas a more inclusive test with a greater number of schools did find an intervention effect. On the basis of this inconsistency, it is still plausible that there is a promising signal that Sources of Strength may reduce suicide deaths of students in future larger trials. However, we reiterate that larger scale public health-oriented designs (state-wide rollouts) are likely required before definitive claims can be made about this intervention’s efficacy for reducing mortality.

An additional caveat is that trial 2 (ie, implementation-effectiveness RCT) suggested that Sources of Strength delivered with low implementation fidelity may have limited or even adverse impact on suicidal behaviour among younger cohorts. It is therefore possible that this programme delivered with low implementation fidelity could produce similar problems for suicide deaths. With this caveat in mind, future roll-out trials should carefully consider behavioural outcomes including suicide deaths and their ongoing relationship to implementation fidelity.

Across multiple populations, suicide decedents are known to be systematically different from individuals who seriously consider or make non-lethal suicide attempts,17 18 therefore identifying interventions that reduce youth suicide mortality is an important independent priority. Prior to this study, no universal intervention has shown reduction in youth suicide mortality through an RCT. The present findings add to evidence that Sources of Strength and other network-based interventions that modify peer and adult relationship systems are a uniquely promising strategy and now worthy of even broader population roll-out studies.

Ethics statements

Patient consent for publication

Ethics approval

This study involves human participants and was approved by Study #1: University of Rochester Medical Center RSRB#20043Study #2: University of Rochester Medical Center RSRB#32551Study #3: University of Florida IRB# IRB201702833. Waiver of documentation of parent permission was used - parents had the opportunity to opt-out students from participating in surveys. Students were informed about study and were told participation was voluntary.



  • Twitter @DrPeterWyman

  • Contributors Study conception and design: all authors. Funding acquisition: PW, CHB, DE and TK. Data collection and analysis: all authors. Manuscript drafting: PW, IC, CHB and KS-C. Manuscript revision and editing: all authors. Guarantor: PW.

  • Funding The three RCTs were supported as follows. Trial #1 was supported by the Center for Mental Health Services (SAMHSA; grant 5-UD1-SM57405), the National Institutes of Health (grants P20MH071897, RO1MH40859, and UL1-RR024160), the New York State Office of Mental Health, and the JDS Foundation. Trial #2 was supported by National Institutes of Health grant RO1MH091452. Trial #3 was funded by the National Center for Injury Prevention and Control (U01CE002841). IC’s time was supported by a grant (KL2 TR001999) from National Center for Advancing Translational Sciences (NCATS) at the National Institutes of Health (NIH) and by a National Institutes of Health Extramural Loan Repayment Award for Clinical Research (L30 MH120727).

  • Disclaimer The funders had no role in the design of the study; in the collection, analyses, or interpretation of data, in the writing of the manuscript, or in the decision to publish the results.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.