Actively Recruiting

Phase Not Applicable
Age: 18Years - 72Years
FEMALE
Healthy Volunteers
NCT05658341

Program of Physical Activity, Nutrition and Supportive to Improve the Quality of Life of Breast Cancer Survivors

Led by Siel Bleu · Updated on 2025-07-16

160

Participants Needed

8

Research Sites

164 weeks

Total Duration

On this page

Sponsors

S

Siel Bleu

Lead Sponsor

I

Institut National de la Santé Et de la Recherche Médicale, France

Collaborating Sponsor

AI-Summary

What this Trial Is About

Despite it being one of the leading causes of cancer death among women, survival following a breast cancer diagnosis has greatly increased in high-income countries. However; this gave rise to a growing population of women living long after breast cancer with a diminished quality of life (QoL) due to the long-term effects of cancer and cancer treatment. Exercise can improve QoL, fatigue, and other mental and physical health outcomes in this population, and is strongly recommended among breast cancer survivors, much like a healthy diet. However adherence in real-life to these recommendations is seldom satisfactory. Also, evidence regarding the effect and cost-effectiveness of concurrent healthy lifestyle behaviors compared to exercise alone is limited. Hence the need to develop pragmatic (evaluating the effectiveness of interventions in real-life conditions) theoretical-based customized interventions, which aim to improve uptake and instill long-term adherence of health lifestyle among breast cancer survivors. ADA (Activité physique adaptée Doublée d'un Accompagnement spécifique post-cancer) is an integrative intervention based on physical activity, nutrition and supportive care. The interventions aims to improve breast cancer survivors' physical and mental health and instill long-term healthy behaviors. Our study will be a pragmatic two-arm (ADA intervention versus control/usual care) cluster randomized controlled trial which examines the effectiveness of the ADA intervention program. The primary endpoint will be health-related quality of life, as measured at 12-month after the start of the trial. Several secondary outcomes will also be assessed; which include Physical activity level, relationship to food and self-efficacy. The study aims to recruit 160 participants in total, divided into 20 activity groups (clusters) of 8 participants. Primary analyses will be carried out on an intention to treat (ITT) basis, at both cluster and participant level. All statistical analysis will adjust for the clustering of patients within centers as a random effect. The aim of this trial is to provide scientific evidence on the 'real-world' effectiveness of an easily generalizable trial, with clinically-significant outcomes, touching a growing number of cancer survivors.

CONDITIONS

Official Title

Program of Physical Activity, Nutrition and Supportive to Improve the Quality of Life of Breast Cancer Survivors

Who Can Participate

Age: 18Years - 72Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult women aged 18 to 72 years
  • Diagnosed with localized breast cancer and completed treatment within the last 15 months, or currently on hormone therapy or nearing the end of Herceptin treatment
  • French-speaking
  • Covered by French Social Security or similar health insurance
Not Eligible

You will not qualify if you...

  • Diagnosis of cancer other than breast cancer, breast cancer relapse, metastasis, or generalized cancer
  • Medical contraindication to exercise requiring a medical certificate
  • Significant visual, hearing, or behavioral problems interfering with group physical activity
  • Planning to move away from the study site
  • Currently participating in another clinical trial
  • Male sex

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 8 locations

1

La Rochelle

La Rochelle, Charentes-maritimes, France, 17

Actively Recruiting

2

Saint Brieuc

Saint-Brieuc, Cotes d'Armor, France, 22

Actively Recruiting

3

Arpajon

Arpajon, Essonne, France, 91

Actively Recruiting

4

Brest

Brest, Finistere, France, 29

Actively Recruiting

5

Blagnac

Blagnac, Haute Garonne, France, 31

Actively Recruiting

6

Angers

Angers, Maine Et Loire, France, 49

Active, Not Recruiting

7

Pyrénées Atlantiques

Saint-Pée-sur-Nivelle, Pyrénées Atlantiques, France, 64

Suspended

8

La Roche sur Yon

La Roche-sur-Yon, Vendée, France, 85

Actively Recruiting

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Research Team

N

Nicolas Deschamps

CONTACT

G

Gwenn Menvielle, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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