Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06207084 · ClinicalTrials.gov registry record · NA

The Fit With Us Study

A NA study of Physical Activity and Fatigue, sponsored by University of Alabama at Birmingham.

Recruiting
Registry status
NA
Development phase
257
Enrollment target
1
Study location

NCT06207084: Recruiting NA study of Physical Activity and Fatigue, sponsored by University of Alabama at Birmingham.

NCT06207084 is a NA study of Physical Activity and Fatigue that is actively recruiting participants, run by University of Alabama at Birmingham. The registered enrollment target is 257 participants, below the 356-participant average among 131 other Physical Activity trials with a reported enrollment target (28% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06207084, a NA study of Physical Activity and Fatigue, is actively recruiting participants, sponsored by University of Alabama at Birmingham.

RECRUITING
Registry status
NA
Development phase
257 participants
Enrollment target
1
Study location

Study 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 a 24-week maintenance phase (weeks 9-32). The study outcomes are: The effectiveness of the adaptive interventions; Exploring mediating and moderating variables; Sensitivity analysis of the predictive analytics.

Primary Outcome

The primary outcome is the change in physical activity (steps per day) from baseline to the end of the 32-week intervention. Participants wear Fitbit Inspire 3 trackers (Google LLC, Sacramento, CA) for continuous objective measurement, with data exported via the study dashboard. This is supplemented by the Godin Leisure-Time Exercise Questionnaire (GLETQ) at baseline, week-8 and week-16 for self-reported leisure-time activity in MET-minutes/week.

Conditions Studied

Physical Activity Fatigue Self Efficacy Behavior, Health Disability Physical Health Literacy Telehealth eHealth Mobility Limitations Health Coaching

Interventions

  • BEHAVIORAL asynchronous content only
  • BEHAVIORAL Asynchronous content and health coaching and no live training
  • BEHAVIORAL asynchronous content only and 1 on 1 live training
  • BEHAVIORAL asynchronous content and health coaching and 1 on 1 training
  • BEHAVIORAL asynchronous content and group training

Study Locations (1)

Alabama

  • Wellness, Health and Research Facility - Birmingham

Trial Details

FieldValue
Enrollment Target 257 participants
Start Date 2024-09-01
Est. Completion 2029-02-01
Phase NA
University of Alabama at Birmingham

1,160 total trials

What NCT06207084 shows while recruiting

NCT06207084 is an interventional study that assigns participants to a tested intervention. The registered 257 participants enrollment target is mid-sized for trials with a published cap, below the 356-participant average among 131 other Physical Activity trials with a reported enrollment target (28% lower).

The record links to 10 conditions, with Physical Activity appearing as the primary indexed condition, and to 5 interventions - of which asynchronous content only is the first listed.

NCT06207084 reports a single indexed study location in Alabama.

Frequently Asked Questions

What is clinical trial NCT06207084 about?

NCT06207084 is a clinical study titled "The Fit With Us Study". 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 a...

What is the current status of trial NCT06207084?

This trial is currently recruiting. It is a NA study. The enrollment target is 257 participants. The study started on 2024-09-01. Estimated completion is 2029-02-01.

What conditions does trial NCT06207084 study?

This clinical trial studies the following conditions: Physical Activity, Fatigue, Self Efficacy, Behavior, Health, Disability Physical.

What interventions are being tested in trial NCT06207084?

The interventions under investigation include: asynchronous content only (BEHAVIORAL), Asynchronous content and health coaching and no live training (BEHAVIORAL), asynchronous content only and 1 on 1 live training (BEHAVIORAL), asynchronous content and health coaching and 1 on 1 training (BEHAVIORAL), asynchronous content and group training (BEHAVIORAL).

Who is sponsoring clinical trial NCT06207084?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06207084 being conducted?

This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Learn More About Clinical Trials

Similar trials for Physical Activity

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06207084's enrollment target sits among peer trials

257 43rd of 131 higher than 89 of 131 other Physical Activity trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Physical Activity trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03618550 · 257 participants · Phase 2

    Phase II Study of Second- Line Pembrolizumab Plus GVD for Relapsed or Refractory Hodgkin Lymphoma

  • NCT04674267 · 257 participants · NA

    Resilience and Equity in Aging, Cancer, and Health (REACH)

  • NCT06099288 · 257 participants · NA

    Strong Families Start at Home/Familias Fuertes Comienzan en Casa

  • NCT03785288 · 258 participants · Phase 3

    Vaginal Cuff Brachytherapy Fractionation Study

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

More recruiting context for NCT06207084

Source: ClinicalTrials.gov NCT06207084, the US trial registry maintained by the National Library of Medicine. NCT06207084 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.