Trials / Completed
CompletedNCT03917901
Computer-Delivered Intervention for Individuals With Obesity and Elevated Anxiety Sensitivity
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 131 (actual)
- Sponsor
- University of Houston · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The proposed study will design and evaluate a computerized-delivered single-session anxiety sensitivity reduction program (i.e., Anxiety Sensitivity Training; AST). The AST will be designed to achieve three primary aims: (1) provide psycho-educational information on AS and its consequences, (2) present psycho-educational information on the relationship between AS and obesity-related health behavior correlates, and (3) offer concrete, evidence-based strategies to facilitate motivation to change their obesity-related lifestyle behaviors.
Detailed description
The primary goal of the research study is to investigate the efficacy of a brief, computer-delivered transdiagnostic intervention that addresses anxiety sensitivity to reduce emotional eating, eating expectancies, food cravings, binge eating, perceived barriers to engage in physical activity, anxiety/depressive symptoms, severity of daily fatigue and increase perceived benefits to engage in physical activity, exercise self-efficacy, willingness to use adaptive coping strategies, and perceived physical health functioning. To address this aim, the investigator's will implement a randomized controlled trial that will employ a longitudinal experimental design and involve five stages: (a) online pre-screener; (b) baseline survey consisting of a pre-intervention assessment (eligibility) and random assignment to a one-session computer-delivered intervention (Active versus Control); (c) 1-week follow-up survey; (d) 2-week follow-up survey; (e) 1-month follow-up survey.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Anxiety Sensitivity Training | Computerized Single-Session Anxiety Sensitivity Reduction Program |
| OTHER | Health Control | Computerized Single-Session Health Information Control |
Timeline
- Start date
- 2019-09-16
- Primary completion
- 2021-03-06
- Completion
- 2021-03-06
- First posted
- 2019-04-17
- Last updated
- 2024-08-26
- Results posted
- 2024-08-26
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT03917901. Inclusion in this directory is not an endorsement.