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NCT05946187Active, not recruiting

Alternative Healthcare Delivery Strategies to Prevent Weight Regain After Bariatric Surgery

Getting Back on Track: Alternative Healthcare Delivery Strategies to Prevent Weight Regain After Bariatric Surgery

Source: ClinicalTrials.gov · Last updated 11 Dec 2024

Brief summary (registry, in English)

Bariatric surgery is the most effective treatment for severe obesity, yet a significant percentage of patients achieve suboptimal results or present long-term weight regain. Given the strong association between poor outcomes and post-surgery psychological factors, it is crucial to implement post-surgical psychological interventions. This randomized controlled trial aims to compare the efficacy of a novel, cost-effective, and timely-personalized treatment delivering strategy (stepped-care) with two different intensities 1) low-intensity intervention delivered by Facebook®, and 2) high-intensity program delivered online. It is also intended to study predictors, outcome moderators/mediators, and the underlying mechanisms of weight regain. Participants' assessment will include measures of pathological eating behavior, psychological impairment, negative urgency, and emotional regulation.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
144 (estimated)
First submitted
24 May 2023
Start date
1 May 2022
Primary completion date
30 Nov 2024
Lead sponsor
University of Minho
Diseases
Obesity
NCT number
NCT05946187

What you commit to

  • Study type: Interventional
  • Planned participants: 144
  • From 1 May 2022 to the primary completion date, 30 Nov 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

  • Under weight-loss medications;

Other illness

  • Having acute psychiatric or medical problems;

Other

  • pregnancy or lactation;
  • illiteracy.

Who the study is looking for

  • Underwent Roux-en-Y Gastric Bypass or Gastric Sleeve
  • Be at least 12 months after surgery;
  • Have a Facebook® account and regular Internet access.

Age in the registry: 18 years to 65 years · Sex: Female · 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
Centro Hospitalar Universitario do Porto
Coordinator of this site? Confirm its status
PortoPortugalUnknown status

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