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NCT04036331 · ClinicalTrials.gov registry record · NA
Dyad Plus Effectiveness/Feasibility
A NA study of Weight Loss and Pediatric Obesity, sponsored by Wake Forest University Health Sciences.
- Recruiting
- Registry status
- NA
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT04036331 is a NA study of Weight Loss and Pediatric Obesity that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 90 participants, below the 1,501-participant average among 116 other Weight Loss trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04036331, a NA study of Weight Loss and Pediatric Obesity, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.
- RECRUITING
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research is to determine the effectiveness of a coordinated program (Dyad Plus) that would help to facilitate self-monitoring, positive communication, joint problem solving, and social support to increase physical activity, healthy eating, and weight loss. Participants of the Brenner FIT (Families In Training) pediatric weight management program and their parent/guardian will co-enroll in weight loss programs. Parents/guardians will receive the components of By Design Essentials.
Conditions Studied
Interventions
- BEHAVIORAL Brenner FIT Standard
- BEHAVIORAL By Design Essentials
- BEHAVIORAL Dyad Plus
Study Locations (1)
North Carolina
- Wake Forest Baptist Medical Center - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2021-07-30 |
| Est. Completion | 2026-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04036331
The ClinicalTrials.gov registry entry for NCT04036331 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,501-participant average among 116 other Weight Loss trials with a reported enrollment target (94% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Weight Loss appearing as the primary indexed condition, and to 3 interventions - of which Brenner FIT Standard is the first listed.
NCT04036331 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT04036331 about?
NCT04036331 is a clinical study titled "Dyad Plus Effectiveness/Feasibility". The purpose of this research is to determine the effectiveness of a coordinated program (Dyad Plus) that would help to facilitate self-monitoring, positive communication, joint problem solving, and social support to increase physical activity, healthy eating, and weight loss. Participants of the Bre...
What is the current status of trial NCT04036331?
This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2021-07-30. Estimated completion is 2026-03.
What conditions does trial NCT04036331 study?
This clinical trial studies the following conditions: Weight Loss, Pediatric Obesity, Parent-Child Relations, Overweight Adolescents, Family and Household.
What interventions are being tested in trial NCT04036331?
The interventions under investigation include: Brenner FIT Standard (BEHAVIORAL), By Design Essentials (BEHAVIORAL), Dyad Plus (BEHAVIORAL).
Who is sponsoring clinical trial NCT04036331?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04036331 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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