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Digital Phenotyping in Women Over 70 Years of Age Treated for Breast Cancer With Any Type of Treatment (GrannyFit)

I

Institut Curie

Status

Active, not recruiting

Conditions

Breast Cancer

Treatments

Device: Activity tracker

Study type

Interventional

Funder types

Other

Identifiers

NCT05634395
IC 2021-08

Details and patient eligibility

About

GrannyFit is a prospective, national, multicenter, single-arm open-label study. It will include a total of 200 participants over the age of 70 years treated for de novo or recurrent (local or distant) BC. Participants will receive a Withing Steel activity tracker, which they will be asked to wear 24 h per day for 12 months. The principal assessments will be performed at baseline, at 6 months and at 12 months. The investigators will evaluate clinical (e.g. comorbidities), lifestyle, quality of life, fatigue, and physical activity parameters. All questionnaires will be completed on a REDCap form, via a secure internet link.

Full description

BACKGROUND: In metropolitan France in 2017, 58,968 new cases of breast cancer (BC) were estimated, of which 25,283 (46.7%) involved women older than 65 years. Older patients with cancer often present complex health needs, in particular because of the burden of comorbidities combined with the effects of aging, the cancer and its treatments. GrannyFit aims to use an activity tracker to identify and describe various digital profiles (physical activity, sleep) in women over 70 years of age treated de novo or recurrent (local or distant) BC.

METHODS: GrannyFit is a prospective, national, multicenter, single-arm open-label study. It will include a total of 200 participants over the age of 70 years treated for de novo or recurrent (local or distant) BC. Participants will receive a Withing Steel activity tracker, which they will be asked to wear 24 h per day for 12 months. The principal assessments will be performed at baseline, at 6 months and at 12 months. The investigators will evaluate clinical (e.g. comorbidities), lifestyle, quality of life, fatigue, and physical activity parameters. All questionnaires will be completed on a REDCap form, via a secure internet link.

DISCUSSION: GrannyFit will make it possible, through the use of an activity tracker, to visualize changes, over a one-year period, in the lifestyle of older BC patients. This study identify more precisely the unmets needs of this population and optimize their care through specific paths. This trial will also pave the way for interventional studies on physical activity and sleep interventions in this population.

Enrollment

200 estimated patients

Sex

Female

Ages

70+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women over 70 years of age,
  • With histologically confirmed invasive breast cancer,
  • Regardless of histological subtype (hormone receptor positive (HR+), negative (HR-), with or without HER2 overexpression, or triple negative)
  • Treated with local (surgery, radiotherapy) or systemic (hormone therapy, monotherapy, anti HER2, chemotherapy: patient is eligible for inclusion up to one month after initial diagnosis or recurrence (local or distant) of breast cancer,
  • PS ≤ 2,
  • Willing and available to invest in the project for the duration of the study,
  • Using a personal smartphone or personal tablet compatible with the "Withings Health Mate" app (iOS 10/android 5.0 and later) and with an internet connection,
  • Affiliated with a social security plan,
  • Having dated and signed an informed consent,
  • Able to read, write and understand French.

Exclusion criteria

  • Presence of disabling metastases,
  • Moderate to severe cognitive impairment,
  • Persons deprived of liberty or under guardianship,
  • Inability to undergo the medical follow-up of the trial for geographical, social or psychological reasons,

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Intervention with activity tracker
Experimental group
Description:
Women allocated to the intervention arm will used an activity tracker
Treatment:
Device: Activity tracker

Trial contacts and locations

4

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Central trial contact

Fabien Reyal, MD; Jean-Guillaume Feron, MD

Data sourced from clinicaltrials.gov

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