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NCT06922630Active, not recruiting

WIN: a Feasibility Study of a Weight-Neutral Health Intervention

WIN: a Feasibility Study of a Weight-Neutral Health Intervention. Lighthouse Consortium on Obesity Management (LightCOM) Trial no 1.

Source: ClinicalTrials.gov · Last updated 4 Dec 2025

Brief summary (registry, in English)

The WIN intervention aims to improve the mental, social and physical health as well as quality of life of participants with BMI≥30 without focusing on their weight, and with no aim of weight loss. The WIN 6 months intervention is based on the principles and methods of the weight neutral movement Health at Every Size (HAES). The content is developed in a co-design process that involved Danish participants who have lived or professional experiences with such approaches. The intervention uses the method of intuitive eating to align eating behaviours with internal cues of hunger and fullness rather than rules, restrictions and external cues. The intervention also draws on components from Acceptance and Commitment Therapy (ACT) to manage body image concerns and weight stigma.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
56 (estimated)
First submitted
3 Apr 2025
Start date
7 Aug 2025
Primary completion date
31 Dec 2026
Lead sponsor
Carsten Dirksen
Diseases
Obesity
NCT number
NCT06922630

What you commit to

  • Study type: Interventional
  • Planned participants: 56
  • From 7 Aug 2025 to the primary completion date, 31 Dec 2026
  • 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

  • Has used weight loss medications or GLP-1 agonist treatment within the past 6 months or intends to use weight loss medications or begin any other intensive weight loss treatment during the WIN intervention.

Other illness

  • Has severe psychiatric or physical conditions that may interfere with participation or may present a safety concern.

Other

  • Intends to become pregnant during the intervention or is currently pregnant.
  • Cannot transport themselves to the group sessions.
  • Is deemed unable to complete a two-hour group session, as assessed by the investigator at the clinical screening interview.
  • Takes part in other research involving weight loss treatment that would compromise participation in this study.

Who the study is looking for

  • Age ≥18 years old at screening.
  • BMI ≥30 kg/m2.
  • Residence in the Capital Region of Denmark.
  • Able to understand and communicate in Danish.
  • Informed consent.

Age in the registry: 18 years to - · 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
Research Unit for General Practice and Section of General Medicine, Department of Public Health, University of Copenhagen
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status

Related publications

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