Clin2
NCT06925269Worth exploringRecruiting

DMD Voice: Interviews with patients and caregivers

Duchenne Muscular Dystrophy (DMD)

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This study invites people with Duchenne muscular dystrophy (DMD) and their caregivers to share their experiences through interviews. It focuses on those who have been taking the medication Givinostat for at least two years, or caregivers of patients with limited arm movement.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
68 people
Ages
10 years and older
Study type
Observational

Who can take part

  • You are a Duchenne muscular dystrophy (DMD) patient age 10 or older, or a caregiver of someone with DMD.
  • If you are a patient, you must have been taking Givinostat for at least 2 years and still be taking it now.
  • If you are a caregiver, you must be a parent or legal guardian of a DMD patient who has been on Givinostat for 2+ years, or care for a DMD patient who cannot lift their hands above their head.
  • You must be willing to take part in a video or audio recorded interview.
  • Caregivers in the second group must live in the U.S. or Canada, speak English, and have a stable internet connection.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT07423026Recruiting
Remote study using technology to track DMD in young boys

This study uses remote technology, like apps or wearable devices, to monitor motor skills and development in boys with Duchenne muscular dystrophy (DMD). It aims to find better ways to measure how the disease progresses over time without requiring frequent clinic visits.

Oxford
NCT07609394Recruiting
Duchenne and Becker Muscular Dystrophy Health Records Study

This study collects electronic health records (medical information already in your doctor's computer system) from people with Duchenne or Becker muscular dystrophy, or female carriers of these conditions. Researchers will use this data to better understand the diseases and improve care over time.

Little Rock, Arkansas
NCT07286565Recruiting
Remote motor development study for early-diagnosed DMD or SMA

This study remotely tracks motor development in children with Duchenne muscular dystrophy or spinal muscular atrophy who were diagnosed at birth or before symptoms started. It aims to see if early monitoring helps improve long-term care and outcomes.

Liège
NCT07402122Not yet recruiting
Registry for Duchenne and Becker muscular dystrophy

This study collects information from patients with Duchenne or Becker muscular dystrophy to learn more about the conditions and improve care. You will share data through a telemedicine platform, and you need a smartphone or tablet to take part.

Essen
NCT07092540Recruiting
Baby Duchenne Study: Early Years in Boys With DMD

This study tracks development and health in young boys with Duchenne muscular dystrophy during the first three years of life. It aims to better understand early signs and how the condition progresses, which may help improve care and future treatments.

Rochester, New York
NCT07664124Not yet recruiting
Digital arm monitoring for non-walking Duchenne

This study tests a wrist-worn sensor (Syde) to track arm and hand movement in boys with Duchenne who cannot walk. The goal is to see if the sensor can help doctors monitor changes in arm function over time, which may help guide future care.

Liège

Hear when a new Duchenne Muscular Dystrophy (DMD) trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.