Adaptation of an Evidence-based Interactive Obesity Treatment Approach (iOTA) for Obesity Prevention in Early Serious Mental Illness: iOTA-eSMI
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Obesity
- Sponsor
- Washington University School of Medicine
- Enrollment
- 51
- Locations
- 2
- Primary Endpoint
- Body Mass Index
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
Using a design-for-dissemination approach, this application proposes to use combined methods to adapt and pilot test an interactive obesity treatment approach (iOTA) for obesity prevention in early serious mental illness (eSMI) that uses text messaging to provide between-visit support. Derived from the lifestyle intervention used in the Diabetes Prevention Program, the parent iOTA targets diet, activity and adherence using web-based and health coach support.
Detailed Description
Most obesity and related complications in serious mental illness (SMI) occur in the context of chronic psychiatric illness, but there are few treatments that work. Behavioral interventions face challenges with long-term effectiveness, implementation and sustainability. Medications have modest effectiveness at best, and/or pose serious side effect risks. This study focuses on prevention of chronic obesity by adapting and pilot testing a prevention-focused, interactive obesity treatment approach (iOTA) for use in persons with early-phase SMI (eSMI) experiencing initial weight gain, overweight or early-stage obesity. The intervention will be adapted from the most studied, effective iOTA, derived from the Diabetes Prevention Program. The parent iOTA uses health coaches who extend their sustainable reach with scalable, inexpensive, semi-automated text messaging. Using a formal evaluation process and a specific implementation science framework, planned adaptations for this application will address mechanisms to improve health-related awareness, insight and self-efficacy skills. Aim 1: Evaluate barriers and facilitators for intervention engagement, effectiveness and implementation, and identify needed adaptations of the prior iOTA for use in obesity attenuation in eSMI. Aim 2: Adapt the prior iOTA for use in obesity attenuation in eSMI, aiming to maximize acceptability, engagement, sustainable reach and target engagement for eSMI. Aim 3: Conduct a randomized pilot and feasibility study of iOTA-eSMI in a diverse sample of adults aged 18-45 with eSMI and initial weight gain, overweight or early class I obesity, comparing iOTA-eSMI to a health education condition.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age 18-60 years
- •At-risk weight defined as greater than 7 percent weight gain in the prior 2 years, overweight as evidenced by BMI 25-29.9, OR class I obesity as evidenced by BMI 30-32.49
- •Serious Mental Illness diagnosis
- •Receiving case management services
- •University of California, San Diego Brief Assessment of Capacity to Consent score less than 14
- •Not taking weight loss medications or participating in another behavioral weight loss intervention
- •Mild to moderate psychiatric symptom severity as measured by the Clinical Global Impression Severity scale
- •Willing and able to provide written informed consent
- •Exclusion criteria:
- •Taking weight loss medications or participating in another behavioral weight loss intervention
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Body Mass Index
Time Frame: baseline and 24 weeks
weight in kilograms/height in meters squared
Secondary Outcomes
- Change in Self-Efficacy for Diet and Exercise(Baseline and 24 weeks)
- Change in Psychophysical Skills & Insight(Baseline and 24 weeks)