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NCT04922216Completed

Adaptive Goals and Interventions for Lifestyle Enhancement

Optimization of a mHealth Behavioral Weight Loss Intervention for Young Adults

Source: ClinicalTrials.gov · Last updated 20 Jul 2025

Brief summary (registry, in English)

Mobile obesity interventions have the potential to reach a diverse population in need; however, while effective, have not resulted in weight losses obtained in in-person interventions. Newer digital approaches called Just-in-Time Adaptive Interventions (JITAI) that offer adaptive, personalized feedback 'when needed' and in 'real time' offer an opportunity to use digital health tools "just in time". This study seeks to identify the optimal components of a comprehensive weight loss JITAI that results in weight losses that meet or exceed those in existing remotely delivered interventions.

Status (registry)
Completed
Study type
Interventional
Enrollment
759 (actual)
First submitted
4 Jun 2021
Start date
28 Apr 2022
Primary completion date
20 Jun 2024
Lead sponsor
University of North Carolina, Chapel Hill
Diseases
Obesity
NCT number
NCT04922216

What you commit to

  • Study type: Interventional
  • Participants enrolled: 759
  • From 28 Apr 2022 to the primary completion date, 20 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Type 1 diabetes or currently receiving medical treatment for Type 2 diabetes
  • Currently taking weight loss medications

Other illness

  • Other health problems which may influence the ability to walk for physical activity or be associated with unintentional weight change, including cancer treatment within the past 5 years or tuberculosis
  • Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q; items 1-4)
  • Report a past diagnosis of or current treatment for a DSM-V (Diagnostic and Statistical Manual 5) eating disorder (anorexia nervosa or bulimia nervosa)
  • Hospitalization for depression or other psychiatric disorder within the past 12 months
  • History of psychotic disorder or bipolar disorder

Other

  • Lost 10 or more pounds (and kept it off) in the last 6 months
  • Currently pregnant, pregnant within the past 6 months, or planning to become pregnant within the next 6 months
  • Another member of the household is a participant or staff member on this trial
  • Currently participating in a weight loss, nutrition or physical activity study or program or other study that would interfere with this study

Who the study is looking for

  • body mass index (BMI) of 25-45 kg/m\^2
  • English-speaking and writing
  • own a smartphone with a data and text messaging plan
  • willing to be randomized to any levels of the factors

Age in the registry: 18 years to 39 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of North Carolina at Chapel Hill
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.