Implementation Support for Prevention Program Delivery by College Peer Educators (PI)

Oregon Research Institute

Status: Completed

Conditions: Eating Disorder

Treatments: Behavioral: Training; Behavioral: Training and Technical Assistance; Behavioral: Training, Tech. Assistance, Quality Assurance/Improvement

Study type: Interventional

Funder types: Other

Identifiers

NCT03409809

MH112743

Details and patient eligibility

About

This project will evaluate 3 approaches of implementation support for university peer leaders who will deliver a prevention program with a particularly strong evidence-base compared to changes observed in outcomes in response to usual care at the universities before implementation. This study aims to advance knowledge of this innovative and economical way to provide college prevention programs to reduce the burden of mental illness in the college student population.

Full description

Several interventions for mental health problems are efficacious and effective, but few are routinely offered to college students, who represent 59% of young adults. This is regrettable because college students are at high risk for mental health problems (e.g., depression, substance abuse, eating disorders), and college counseling centers lack sufficient clinicians to offer individual therapy to all afflicted students and are not well positioned to deliver prevention programs. One solution for this service shortfall is to have peer educators deliver scripted group-based prevention programs, which can more efficiently reduce the burden of mental illness than individual therapy. Targeting college students is a cost-effective tactic for delivering prevention programs and has vast potential reach because 85% of colleges have peer educator programs. Peer educators have effectively delivered several prevention programs, sometimes producing larger effects than clinicians. This study will investigate 3 levels of implementation support (training, training with technical assistance, and training with technical assistance and quality assurance) and the impacts of differing levels of implementation support on program outcomes across 57 college campuses nationwide. Specifically we have five aims for this study:

Aim 1: Test whether greater implementation support is associated with graded increases in fidelity and competence in delivering the scripted prevention program. This will be assessed by an established procedure for reliably rating fidelity and competence of audio-recorded intervention sessions.

Aim 2: Test whether greater implementation support, which should increase fidelity and competence of intervention delivery, is associated with graded increases in student attendance of intervention sessions (recorded by the peer educators) and effectiveness of the prevention program (measured by pre-to-post changes in core outcomes assessed with anonymous surveys completed by group participants) and compared to parallel pre-to-post change data collected from students at the colleges before implementation is initiated.

Aim 3: Test whether greater implementation support is associated with graded increases in program reach (% of female students at each college who complete the prevention program during the 1-year implementation period) and sustainability (% of female students at each college who complete the prevention program during the subsequent 2-year sustainability monitoring period).

Aim 4: Test whether Consolidated Framework for Implementation of Research (CFIR) indices of perceived intervention factors, outer and inner setting factors, peer educator attributes, and process factors after the initial training correlate with fidelity, competence, attendance, effectiveness, and reach over the 1-year implementation period and with sustainability. We will test whether at the end of the initial implementation period the 3 conditions differ on relevant CFIR indices and on the progress and speed of implementation.

Aim 5: Compare the prevention program delivery cost in the 3 implementation conditions, and the relative cost-effectiveness of each condition in terms of attaining fidelity, competence, attendance, and effectiveness, reach, and sustainability, plus cost-savings from and reductions in waitlists and eating disorder prevalence at clinics.

Starting in March of 2020, virtually-hosted Body Project groups are being recommended to participating Peer Education teams in contexts where in-person groups can not be offered due to COVID-19 social distancing guidelines. Existing research indicates that virtual Body Project groups are a viable and effective alternative in-person groups.

Enrollment: 2,261 patients

Sex: All

Ages: 17+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Five Categories of Study Participant: (1) Peer Educator, (2) Peer Educator Supervisor, (3) Clinician, (4) Body Project Group Participant, (5) Usual Care Participant

1. Peer Educator

   Inclusion Criteria:

   • College undergraduate student Peer Educators with an interest in promoting body satisfaction
   • Willing to attend a 2-day Body Project train-the-trainer (TTT) training

   Exclusion Criteria:

   • Undergraduate college students from a college or university* that does not have a formal Peer Education Program

2. Peer Educator Supervisor

   Inclusion Criteria:

   • College or University* staff members with an interest in promoting body satisfaction
   • Willing to attend a 2-day Body Project train-the-trainer (TTT) training

   Exclusion Criteria:

   • Not a staff member

3. Clinician

   Inclusion Criteria:

   • Clinician working at a US College or University*

   Exclusion Criteria:

   • Not a clinician

4. Body Project Group Participant

   Inclusion Criteria:

   • College* students with an interest in promoting body satisfaction

   Exclusion Criteria:

   • Not a college student

5. Usual Care Participant

Inclusion Criteria:

• College* students with an interest in promoting body satisfaction

Exclusion Criteria:

• Not a College* student

• Current or past participant in a Body Project group

  • Participating students and staff are randomized at the school level.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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2,261 participants in 3 patient groups

Training Alone

Experimental group

Description:

This condition involves an intensive 2-day initial train-the-trainer workshop that simultaneously trains peer educators to deliver the intervention and campus supervisors to train and support future peer educators, plus the facilitator guide and facilitator support website.

Treatment:

Behavioral: Training

Training and Technical Assistance

Experimental group

Description:

This condition involves an intensive 2-day initial train-the-trainer workshop that simultaneously trains peer educators to deliver the intervention and campus supervisors to train and support future peer educators, plus the facilitator guide and facilitator support website. This condition additionally contains a 1/2 day implementation training to articulate goals, needs, leadership structure, adoption options, recruitment strategies, and communication.

Treatment:

Behavioral: Training and Technical Assistance

Training, Tech. Assist., Qual. Assurance

Experimental group

Description:

This condition involves an intensive 2-day initial train-the-trainer workshop that simultaneously trains peer educators to deliver the intervention and campus supervisors to train and support future peer educators, plus the facilitator guide and facilitator support website. This condition additionally contains a 1/2 day implementation training to articulate goals, needs, leadership structure, adoption options, recruitment strategies and communication. Furthermore, this condition will have 1 year of technical assistance, coaching, and quality assurance to enhance implementation skills and sustainability.

Treatment:

Behavioral: Training, Tech. Assistance, Quality Assurance/Improvement