Clinical Trial

Computer-Delivered Intervention in Obesity and Anxiety

Study Description

Computer-Delivered Intervention for Individuals With Obesity and Elevated Anxiety Sensitivity

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.

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Anxiety Sensitivity Training

Computerized Single-Session Anxiety Sensitivity Reduction Program

Health Control

Computerized Single-Session Health Information Control

Additional Information

Official Study Title

Computer-Delivered Intervention for Individuals With Obesity and Elevated Anxiety Sensitivity

Clinical Trial ID

NCT03917901

ParticipAid ID

e31ppb