The Fit With Us Study

Physical Activity Clinical Trial

— FITWITHUS  

Official title:

Precision-based Teleexercise Trial to Increase Adherence in People With Disabilities

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06207084
• Other study ID #: IRB-300011762
• Secondary ID: 90REGE0019
• Status: Not yet recruiting
• Phase: N/A
• Start date: May 1, 2024
• Est. completion date: February 1, 2029

Study information

• Verified date: April 2024
• Source: University of Alabama at Birmingham
• Contact: Mohanraj Thirumalai, PhD
• Phone: 205-934-7189
• Email: mohanraj[@]uab.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this 32 week study is to use an innovative experimental design known as SMART (Sequential Multiple Assignment Randomized Trial), which will allow us to determine the best way to sequence the delivery of teleexercise (referred to as an adaptive intervention), combined with predictive analytics on participant adherence in a stepped program of physical activity interventions.

All 257 participants will have access to a library of recorded video exercise content, and a weekly wellness article. Some participants will receive health coaching calls (1st randomization). Analytic data will be used to determine which participants are responding or not responding to the intervention. Participants not responding after 4 weeks will receive either live one on one or group exercise training (2nd randomization). After 8 weeks, the participant will receive only pre recorded exercise content and articles for another 8 weeks. After final surveys, participants will have open access to the website for another 16 weeks where we will passively observe their fitbit and website data.

The study outcomes are:

The effectiveness of the adaptive interventions Exploring mediating and moderating variables Sensitivity analysis of the predictive analytics

Description:

Our proposed Sequential Multiple Assignment Randomized Trial (SMART) study seeks to develop an effective 32-week, resource sensitive strategy to improve physical activity levels in people with mobility impairments.

During the Run-In period before the start of the intervention, interested individuals will consent to be part of the study. Once providing consent, Participants will respond to a baseline survey packet through RedCap. Additionally, during the run-in period, the research team will ship an exercise tracker device, and a set of wrist weights for the participant to wear during the intervention. The participant will receive an orientation call to assist them with using the website, setting up their exercise tracking device, and linking the device to the website. (see attached call outline)

After the run-in period, participants will be randomized into 1 of 2 groups: Asynchronous Exercise Program (AEP) and AEP + Smart Health Coaching (SHC). Finally, participants will be given access to the Fitwithus online platform, hosted on UAB servers, to access all the exercise content (exercise videos and articles).

The Adoption Phase will be split into two 4-week phases: early adoption (weeks 1 to 4) and late adoption (weeks 5 to 8). Participants in both groups will engage in pre-recorded exercise content. The AEP + SHC group may receive up to 8 health coaching calls.

At the end of the early adoption phase, the participant will complete a short set of questions (See week 4 questionnaire) the research team will classify participants in both groups into either a responder or a non-responder. If a participant is a responder, they will continue with their group assignment through the late adoption phase (AEP only or AEP + SHC). If the participant is a non-responder, they will be randomized a second time into 1 of 2 sub-groups: Live 1-on-1 training or Live group training for the late adoption phase. All live training will occur remotely through ZOOM. Participants in non-responder sub-groups will be asked to participate in their respective live training up to 3 times per week for weeks 5 to 8.

Upon finishing the late adoption phase, all participants will complete another survey packet and a semistructured interview (see interview guide), and receive AEP only for an 8-week Maintenance phase (weeks 9 to 16). Upon completion of week 16, the participant will complete a final survey packet. Participants will receive access to the website and content for another 16 weeks and complete a final survey packet. Throughout the study, we will be collecting data from the participant's exercise tracker. These data include steps and minutes of activity/inactivity. During weeks 16 to 32, Participants will have open access to the website and it's library of exercise content. The research team will continue to collect fitbit data and website analytics (for example video watch minutes). Participants may receive a reminder call to complete 4th week or 8 week surveys. (see attached call outline)

This intervention will be administered in waves of about 33 to 34 participants. The first wave will be a pilot wave. The data generated from this pilot wave will not be included in the final analyses, but serve as a test for the intervention. Additionally, pilot wave participants will be asked to complete semistrucutred interview at the end of both week 8 and week 16.

After completion of the pilot wave, the research team may modify or refine the intervention and submit an amendment to the IRB. After approval is obtained, the remaining intervention waves will proceed. (See attached Pilot Wave Consent)

We will use the following validated measures:

Surveys (see attached)

Demographic and Health History Questionnaire (baseline)

Godin Leisure Time Exercise Questionnaire (GLTEQ)

Patient Reported Outcomes Measurement Information System Short-Form Fatigue (PROMIS SF-F))

Social Cognitive Theory Social Provisions Scale (SPS)

Barriers to Self-Efficacy Scale for Physical Activity (BARSE-PA)

eHealth Literacy Scale (eHEALS)

36-Item Short Form Survey: physical functioning (SF36 PF)

mHealth Application Usability Questionnaire (MAUQ)

Acceptability of Intervention Appropriateness Measure, Intervention Appropriateness Measure, & Feasibility of Intervention Measure.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 257
• Est. completion date: February 1, 2029
• Est. primary completion date: February 1, 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

• age 18 to 64 years have a permanent mobility impairment has internet access can converse in English

Exclusion Criteria:

Significant visual acuity that prevents seeing a computer screen to follow a home exercise program has been exercising for the past 6 months or longer.

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Related Conditions & MeSH terms

• Behavior, Health
• Disability Physical
• eHealth
• Fatigue
• Health Literacy
• Mobility Limitation
• Mobility Limitations
• Physical Activity
• Predictive Model
• Self Efficacy
• Telehealth
• Usability

Intervention

Behavioral:
• asynchronous content only
Receives asynchronous exercise content and no live training
• Asynchronous content and health coaching and no live training
Receives asynchronous content, health coaching and no live training.
• asynchronous content only and 1 on 1 live training
receives asynchronous content and live 1 on 1 training
• asynchronous content and health coaching and 1 on 1 training
receives asynchronous content, health coaching, and live training
• asynchronous content and group training
receives asynchronous content and live group training
• Asynchronous content and health coaching and group training
receives asynchronous content, health coaching, and live group training

Locations

Country	Name	City	State
United States	Wellness, Health and Research Facility	Birmingham	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adherence	Use of live training delivery on adherence	8 weeks
Secondary	effectiveness	effectiveness of health coaching	8 weeks
Secondary	physical activity and fatigue	improvement and maintenance of physical activity and fatigue levels	16
Secondary	cost effectiveness	ompare the cost effectiveness of the four adaptive interventions from the societal perspective which includes both program costs and participant costs.	32