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NCT07515274Not yet recruiting

Evaluation of the Effects of Equicoaching on Social Reintegration Among Young Adults Who Have Been Treated for Cancer

Source: ClinicalTrials.gov · Last updated 13 Apr 2026

Brief summary (registry, in English)

This is a category 2 human research study (RIPH), interventional, single-center, prospective, open-label. The primary objective of this study is to qualitatively assess the effects of equicoaching on social reintegration in young adults who have been treated for cancer. The secondary objectives are to evaluate the contribution of equicoaching to: 1. Self-confidence; 2. Well-being 3. Quality of life Satisfaction with equicoaching will also be evaluated.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
2 Dec 2025
Start date
5 Apr 2026
Primary completion date
30 Sept 2026
Lead sponsor
Centre Leon Berard
NCT number
NCT07515274

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 5 Apr 2026 to the primary completion date, 30 Sept 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.

Other

  • Patient deprived of liberty by judicial or administrative decision
  • Pregnant or breastfeeding women

Who the study is looking for

  • Have been treated for a malignant oncological or hematological condition.
  • Be between 15 and 25 years of age at the time of cancer diagnosis. This age range corresponds to that chosen by the Leon Berard Cancer Center (CLB) and the Institute of Pediatric Hematology and Oncology (IHOPe) for the Adolescents and Young Adults with Cancer (DAJAC) program
  • Have been treated at IHOPe/CLB as part of the DAJAC program
  • Have completed intensive treatment within the last twelve months.
  • Be able to understand, read, and write French
  • Be affiliated with a health insurance plan
  • Have been informed about the study and have given consent
    • For minors:
  • All of the above criteria
  • Parent/legal guardian informed about the study and having given consent

Age in the registry: 15 years to 25 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
CLB
Coordinator of this site? Confirm its status
LyonFranceUnknown status

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