Skip to content

Exercise rehabilitation trial in Huntington'?s disease

A randomised exercise rehabilitation trial in Huntington's disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11392629
Enrollment
26
Registered
2014-01-24
Start date
2014-02-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Dementias and Neurodegenerative Diseases Research Network

Interventions

People with HD who enrol in the study will be asked to attend two research assessments (focussing on physical fitness, movement, thinking and walking abilities) over a three-month period at their loca

Sponsors

Cardiff University (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosis of manifest HD, confirmed by genetic testing 2. Male and female above the age of 18 3. Stable medication regime for four weeks prior to initiation of trial, and anticipated to be able to maintain a stable regime for the course of trial 4. Enrolled in European Huntington Disease Network (EHDN) Registry/ENROLL-HD study

Exclusion criteria

Exclusion criteria: 1. Any physical or psychiatric condition that would prohibit the participant from completing the intervention or the full battery of assessments 2. Inability to independently use the cycle ergometer 3. Unable to understand or communicate in spoken English (UK sites only) 4. Currently involved in any intervention trial or within four weeks of completing an intervention trial 5. Current, regular participation in a structured exercise programme five times per week or more

Design outcomes

Primary

MeasureTime frame
Feasibility in terms of adherence, safety and process. Measures will be taken at baseline and 13 weeks. A follow-up telephone call will be made at 26 weeks to conduct the IPAQ and EQ-5D.

Secondary

MeasureTime frame
Assess benefit including physical fitness, cognitive ability and motor function. Measures will be taken at baseline and 13 weeks. A follow-up telephone call will be made at 26 weeks to conduct the IPAQ and EQ-5D.

Countries

Germany, Netherlands, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 1, 2026