Skip to main content
Clinical Trials/NCT04457128
NCT04457128
Unknown
Not Applicable

Just-in-Time Adaptive Intervention to Reduce Sedentary Behavior

University of Alabama, Tuscaloosa0 sites200 target enrollmentJanuary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University of Alabama, Tuscaloosa
Enrollment
200
Primary Endpoint
Usage
Last Updated
5 years ago

Overview

Brief Summary

The goal of this study is to adapt an evidence-based sedentary behavior reduction intervention for men and women living in Alabama and determine its feasibility, acceptance, and limited efficacy.

Detailed Description

The goal of this study is to adapt an evidence-based sedentary behavior reduction intervention for men and women living in Alabama and determine its feasibility, acceptance, and limited efficacy. Community-based Participatory Research methods will be used to adapt an evidence-based curriculum. The adapted curriculum will be delivered via print-based materials and a mobile phone app developed by an external collaborator.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
August 31, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
University of Alabama, Tuscaloosa
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • • 50 to 75 years old at study enrollment;
  • Currently living in Alabama;
  • Community-dwelling (i.e., not living in an assisted living facility or nursing home);
  • Having access to the internet and a smart phone;
  • Able to perform light-intensity physical activity (i.e., walking);
  • English speaking;
  • Willing to consent to study procedure.

Exclusion Criteria

  • Reporting more than 60 minutes of purposeful physical activity per week;
  • Have an unstable mental condition that prevention study activities. Determined by the Physician Health questionnaire.

Outcomes

Primary Outcomes

Usage

Time Frame: 16 weeks

To percentage of time participants were complying with the study protocol

The Usage, Satisfaction, Ease of use Questionnaire

Time Frame: 16 weeks

Questionnaire that assesses usage, satisfaction, and ease of use of technology. Each subscale has a maximum score of 20, with higher scores indicating a better outcome.

Secondary Outcomes

  • Change in light-intensity physical activity(Week 0 and Week 16)
  • Change in sedentary time(Week 0 and Week 16)

Similar Trials