RECRUITING

Dyad Plus Effectiveness

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Effectiveness of A Coordinated Parent/Child Dyad Weight Loss Intervention:

Quick Facts

Study Start:2021-07-30
Study Completion:2025-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04036331

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:13 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Eligible for enrollment in Brenner FIT and/or By Design Essentials
  2. * Caregiver who lives in the house with a BMI \> 30
  3. * No contraindication for physical activity or caloric restriction
  4. * Must be able to read and write English
  1. * BMI \< 30
  2. * Contraindication for physical activity or caloric restriction
  3. * Cannot read or write English

Contacts and Locations

Study Contact

Camelia R Singletary, MPH
CONTACT
13369992469
crsingle@wakehealth.edu
Justin Moore, PhD
CONTACT
336-716-3702
jusmoore@wakehealth.edu

Principal Investigator

Justin Moore
PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences

Study Locations (Sites)

Wake Forest Baptist Medical Center
Winston-Salem, North Carolina, 27127
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Justin Moore, PRINCIPAL_INVESTIGATOR, Wake Forest University Health Sciences

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-07-30
Study Completion Date2025-07

Study Record Updates

Study Start Date2021-07-30
Study Completion Date2025-07

Terms related to this study

Additional Relevant MeSH Terms

  • Weight Loss
  • Pediatric Obesity
  • Overweight Adolescents
  • Parent-Child Relations
  • Family and Household