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NCT07276230Not yet recruiting

Quality of Life Assessment of Caregivers of Patients With Multiple Myeloma

Quality of Life Assessment of Caregivers of Patients With Multiple Myeloma Participating in a Therapeutic Education Program and Receiving a Supportive Care Needs Evaluation

Source: ClinicalTrials.gov · Last updated 29 Dec 2025

Brief summary (registry, in English)

The diagnosis and treatment of multiple myeloma affect not only the patient but also their family and caregivers. Advances in therapy have transformed the follow-up of patients treated for multiple myeloma. The involvement of informal caregivers has become increasingly essential to ensure adequate home-based care, as most treatments are now delivered on an outpatient basis. Literature reviews suggest that caregivers of cancer patients often face unmet supportive care needs, which in turn negatively impact their quality of life.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
27 (estimated)
First submitted
28 Nov 2025
Start date
1 Feb 2026
Primary completion date
1 May 2027
Lead sponsor
Assistance Publique - Hôpitaux de Paris
NCT number
NCT07276230

What you commit to

  • Study type: Interventional
  • Planned participants: 27
  • From 1 Feb 2026 to the primary completion date, 1 May 2027
  • 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 illness

  • Currently being treated for an acute medical condition

Other

  • Caregiver :
  • Not designated by the patient as the primary caregiver
  • Refusal of the caregiver to participate in the study
  • Under legal protection (guardianship or curatorship)

Who the study is looking for

  • Caregiver :
  • Designated by a patient followed for multiple myeloma during first-line treatment
  • Providing weekly assistance to the patient (e.g., shopping, housekeeping, management of daily living activities, healthcare or hygiene support, etc.)
  • Aged 18 years or older
  • Fluent in French
  • Affiliated with or benefiting from a social security system (excluding state medical aid - AME)
  • Able to provide free, written, and 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
Hématologie clinique - Pitié-Salpêtrière Hospital (APHP)
Coordinator of this site? Confirm its status
ParisFranceUnknown status

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