A virtual learning collaborative to implement health promotion in routine mental health settings: Protocol for a cluster randomized trial

• Published in: Contemporary clinical trials 2019-09, Vol.84, p.105816-105816, Article 105816
• Main Authors: Aschbrenner, Kelly A., Pratt, Sarah I., Bond, Gary R., Zubkoff, Lisa, Naslund, John A., Jue, Kenneth, Williams, Gail, Kinney, Allison, Cohen, Michael J., Godfrey, Marjorie M., Bartels, Stephen J.
• Format: Article
• Language: English
• Subjects: Computer-Assisted Instruction - methods; Cooperative Behavior; Diet; Exercise; Fidelity; Health Behavior; Health Education - methods; Health promotion; Humans; Implementation strategy; Inservice Training; Learning collaborative; Mental Disorders - epidemiology; Mental Health Services - organization & administration; Multicenter Studies as Topic; Patient Compliance; Randomized Controlled Trials as Topic; Serious mental illness; United States - epidemiology; Weight Loss
• ISSN: 1551-7144; 1559-2030
• DOI: 10.1016/j.cct.2019.105816

Despite widespread use of learning collaboratives in health care, few randomized trials have evaluated their effectiveness. The primary aim of this cluster randomized implementation trial is to evaluate the effectiveness of a virtual learning collaborative (VLC) in the implementation of a lifestyle intervention for persons with serious mental illness (SMI) in routine mental health settings, compared to standard individual technical assistance. Forty-eight mental health provider organizations from across the United States will be recruited to participate in the trial. The evidence-based practice to be implemented is the InSHAPE health promotion intervention for persons with SMI. Sites will be stratified by size and randomized to receive an 18-month intensive group-based VLC with monthly learning sessions or individual technical assistance with four scheduled conference calls over 18 months. Sites will be enrolled in three blocks of 16 sites each. The primary outcomes are InSHAPE program participation and fidelity, and participant weight loss; secondary outcomes are program operation, program uptake, participant health behaviors of physical activity and nutrition, organizational change, and program sustainment. Implementation outcomes are measured at 3, 6, 12, 18, and 24 months after the program start-up. Participant-level outcomes are measured at fixed intervals every 3 months after each participant enrolls in the study. This study will determine whether VLCs are an effective implementation strategy among resource-limited providers when the new practice necessitates a shift in mission, scope of practice, type of services delivered, and new financing. ClinicalTrials.gov identifier: NCT03891368 Registered 25 March 2019, retrospectively registered. https://clinicaltrials.gov/ct2/show/NCT03891368?term=NCT03891368&rank=1