Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06393725 · ClinicalTrials.gov registry record · NA
Synchronous vs Asynchronous Remotely Delivered Lifestyle Interventions
A NA study of Obesity, sponsored by University of Connecticut.
- Recruiting
- Registry status
- NA
- Development phase
- 328
- Enrollment target
- 1
- Study location
NCT06393725 is a NA study of Obesity that is actively recruiting participants, run by University of Connecticut. The registered enrollment target is 328 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (60% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06393725, a NA study of Obesity, is actively recruiting participants, sponsored by University of Connecticut.
- RECRUITING
- Registry status
- NA
- Development phase
- 328 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to learn if a group-based digital weight loss program that is delivered asynchronously (via an online platform) is as effective as one that is delivered synchronously (via weekly videoconference meetings). In the asynchronous condition, participants can engage with their group any time 24/7. In the synchronous condition, participants can engage with their group once a week at a videoconference meeting. The main questions it aims to answer are: Will participants in each condition lose about the same amount of weight? Will the participants in the asynchronous condition participate more than those in the synchronous condition? Will the participants in the asynchronous condition feel more connected to each other than those in the synchronous condition? Will the asynchronous condition cost less to deliver per pound lost than the synchronous condition? Participants will: Receive a digital weight loss program that lasts 1 year and then volunteer participants will be selected to lead the group for 1 year following the program, a phase called the "peer-led weight loss maintenance phase." Complete study assessments at baseline, 6, 12, 18, and 24 months.
Conditions Studied
Interventions
- BEHAVIORAL Asynchronous Remote Lifestyle Intervention
- BEHAVIORAL Synchronous Remote Lifestyle Intervention
Study Locations (1)
Connecticut
- University of Connecticut - Storrs
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 328 participants |
| Start Date | 2025-02-06 |
| Est. Completion | 2028-06-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06393725
The ClinicalTrials.gov registry entry for NCT06393725 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 328 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (60% lower). The listed sponsor is University of Connecticut, which has 107 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Obesity appearing as the primary indexed condition, and to 2 interventions - of which Asynchronous Remote Lifestyle Intervention is the first listed.
NCT06393725 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.
Frequently Asked Questions
What is clinical trial NCT06393725 about?
NCT06393725 is a clinical study titled "Synchronous vs Asynchronous Remotely Delivered Lifestyle Interventions". The goal of this clinical trial is to learn if a group-based digital weight loss program that is delivered asynchronously (via an online platform) is as effective as one that is delivered synchronously (via weekly videoconference meetings). In the asynchronous condition, participants can engage with...
What is the current status of trial NCT06393725?
This trial is currently recruiting. It is a NA study. The enrollment target is 328 participants. The study started on 2025-02-06. Estimated completion is 2028-06-30.
What conditions does trial NCT06393725 study?
This clinical trial studies the following conditions: Obesity.
What interventions are being tested in trial NCT06393725?
The interventions under investigation include: Asynchronous Remote Lifestyle Intervention (BEHAVIORAL), Synchronous Remote Lifestyle Intervention (BEHAVIORAL).
Who is sponsoring clinical trial NCT06393725?
This trial is sponsored by University of Connecticut, which has 107 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06393725 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Obesity
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.
-
Metabolic Adaptations to Weight Loss With and Without Exercise
RECRUITING · NA
-
Testing an Integrated PTSD and Weight Management Intervention: A Hybrid Type 1 Trial
RECRUITING · NA
-
Tai Chi as a Novel Strategy to Increase Physical Activity Among Adults Pursuing Metabolic and Bariatric Surgery
RECRUITING · NA
-
Mechanistic and Clinical Outcomes of a Surgical Innovation Aimed at Minimizing GERD Associated With VSG (INNOVATE-VSG)
RECRUITING · NA
-
SMARTer Weight Loss Management
RECRUITING · NA
-
HealthyTogether: RCT of a Dyadic Weight Management Intervention
RECRUITING · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.