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Recruiting NCT04036331

NCT04036331 Dyad Plus Effectiveness/Feasibility

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Clinical Trial Summary
NCT ID NCT04036331
Status Recruiting
Phase
Sponsor Wake Forest University Health Sciences
Condition Weight Loss
Study Type INTERVENTIONAL
Enrollment 90 participants
Start Date 2021-07-30
Primary Completion 2026-07

Eligibility & Interventions

Sex All sexes
Min Age 13 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Brenner FIT StandardBy Design EssentialsDyad Plus

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 90 participants in total. It began in 2021-07-30 with a primary completion date of 2026-07.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

Eligibility Criteria

Inclusion Criteria: * Eligible for enrollment in Brenner FIT and/or By Design Essentials * Caregiver who lives in the house with a BMI \> 30 * No contraindication for physical activity or caloric restriction * Must be able to read and write English Exclusion Criteria: * BMI \< 30 * Contraindication for physical activity or caloric restriction * Cannot read or write English

Contact & Investigator

Central Contact

Camelia R Singletary, MPH

✉ camelia.singletary@advocatehealth.org

📞 13369992469

Principal Investigator

Justin Moore

PRINCIPAL INVESTIGATOR

Wake Forest University Health Sciences

Frequently Asked Questions

Who can join the NCT04036331 clinical trial?

This trial is open to participants of all sexes, aged 13 Years or older, up to 65 Years, studying Weight Loss. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04036331 currently recruiting?

Yes, NCT04036331 is actively recruiting participants. Contact the research team at camelia.singletary@advocatehealth.org for enrollment information.

Where is the NCT04036331 trial being conducted?

This trial is being conducted at Winston-Salem, United States.

Who is sponsoring the NCT04036331 clinical trial?

NCT04036331 is sponsored by Wake Forest University Health Sciences. The principal investigator is Justin Moore at Wake Forest University Health Sciences. The trial plans to enroll 90 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology