Recruiting

Social Support Training

Sponsor:

University of South Carolina

Code:

NCT06662292

Conditions

Physical Activity

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Mobile STRIDES app (psychoeducation features)

Mobile STRIDES app (self-regulation features)

Mobile STRIDES app (social support training features)

Study Details

Brief summary:

The goal of this research is to examine the addition of a digitally delivered social support training approach to an existing digital program designed to promote a physically active lifestyle among self-selected teams of adults who are not meeting physical activity guidelines. The main aims are to:

1. Determine if the social support training intervention promotes significantly greater changes in moderate-to-vigorous intensity aerobic physical activity (such as a brisk walk) as measured by an accelerometer (research grade physical activity measurement device) at 3 months compared to the same intervention without social support training among self-selected teams of adults who are not meeting the physical activity guidelines.
2. Determine if the social support training intervention promotes significantly greater changes in social support, motivation, accountability, and autonomy social support (free from excessive control and encouraging one's free will) at 3 months and 12 months compared to the same intervention without social support training.
3. Determine if the social support training intervention promotes significantly greater changes in moderate-to-vigorous intensity aerobic physical activity as measured by an accelerometer at 12 months compared to the same intervention without social support training.
4. Explore whether social support mediates increased and sustained moderate-to-vigorous intensity aerobic physical activity among the entire sample of participants.

Conditions

Physical Activity

Study ID

NCT06662292

Start date

Aug 28, 2025

Status verified date

Oct, 2025

Completion date

Nov 1, 2028

Anticipated

Primary completion date

Nov 1, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

Participants must:

  • be at least 18 years of age
  • be insufficiently physically active (< 150 minutes per week of moderate-intensity equivalent aerobic physical activity as measured by waist-worn accelerometer (research grade physical activity measurement device) - i.e., sum of time spent in minutes of moderate-intensity activity plus twice the minutes spent in vigorous-intensity activity < 150 minutes per week)
  • be part of a self-selected team of 3-8 individuals each of whom also meet all other eligibility criteria (members of the same household are only eligible to participate if they are on the same team - limit one team per household)
  • have access to a smartphone (Android or iphone operating system-based) with an internet connection
  • report being able to walk at least ¼ mile without stopping
  • be able to provide informed consent
  • complete all screening and baseline questionnaires and activities

Exclusion Criteria:

  • participating in another physical activity study or program
  • are pregnant, breastfeeding, less than 6 months post-partum, or plan to become pregnant during the time frame of the investigation
  • report a medical condition that would affect the safety and/or efficacy of a physical activity program (e.g., terminal illness; uncontrolled heart condition, dementia, bulimia nervosa or binge eating disorder, other significant psychiatric problems, or use of insulin)
  • report conditions that in the judgment of the Principal Investigator would render them unlikely to be able to independently follow the intervention protocol for 3 months, including conditions which might compromise their ability to engage independently with the intervention website materials and wearable physical activity tracker, as well as complete online questionnaires and adhere to wearing an accelerometer

Study Design

Enrollment

300 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

active comparator: Team Program

Teams randomized to this arm will be provided with personal physical activity goals focused on moderate-to-vigorous intensity aerobic physical activity minutes and steps. They will also be provided with a Fitibt wearable smartwatch for self-monitoring physical activity, receive weekly electronic feedback for the first month of the intervention about their physical activity progress, and have access to a mobile-compatible study web app containing behavior change content and physical activity progress information.

experimental: Team+Training Program

Teams randomized to this arm will receive the same intervention as the Team study arm, as well as digitally delivered social support training.

Interventions

Mobile STRIDES app (psychoeducation features)

Twelve theory-based physical activity behavior change lessons/modules during the course of the 3-month intervention.

Mobile STRIDES app (self-regulation features)

Personalized physical activity goals focused on moderate-to-vigorous intensity aerobic physical activity and steps. Physical activity (tracked with a Fitbit wearable smartwatch and synced with the Mobile STRIDES app) tracking component, displaying team and individual progress. Weekly individualized feedback messages crafted by a trained professional for the first month of the intervention.

Mobile STRIDES app (social support training features)

For the experimental group, the Mobile STRIDES app also includes five social support training lessons/modules (during the course of the 3-month intervention) focused on providing guidance related to effective communication when exchanging social support for physical activity within a team. In addition, six team feedback messages will be delivered to respective teams throughout the course of the 3-month intervention to reinforce content taught via the training lessons/modules. A weekly poll will also be administered that complements the social support training lessons, with cumulative results displayed.

Primary outcome measure

  • Change in minutes per week of moderate-to-vigorous intensity aerobic physical activity (MVPA) at 3 months [ Time Frame: Baseline and 3 months ]

Central Contacts and Locations

Central contacts

Locations

University of South Carolina

Recruiting

Columbia, South Carolina, United States, 29208

Contacts

Chelsea Carpenter, PhD

803-766-6275mobilestrides@sc.edu

More Information

Sponsor

University of South Carolina

Last update posted

Oct 15, 2025

Last verified

Oct, 2025

Keywords

  • physical activity
  • exercise
  • adults
  • social support
  • smartphone
  • electronic health
  • mobile health
  • teams

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of South Carolina on 2025-10-15.