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

NCT03917901 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 131

Last updated 2024-08-26

Study results available
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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.

Conditions

  • Obesity
  • Anxiety Sensitivity
  • Eating
  • Physical Activity

Interventions

OTHER

Anxiety Sensitivity Training

Computerized Single-Session Anxiety Sensitivity Reduction Program

OTHER

Health Control

Computerized Single-Session Health Information Control

Sponsors & Collaborators

  • University of Houston

    lead OTHER

Principal Investigators

  • Brooke Kauffman, MA · University of Houston

  • Michael J Zvolensky, Ph.D. · University of Houston

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-16
Primary Completion
2021-03-06
Completion
2021-03-06

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03917901 on ClinicalTrials.gov