Skip to content

Home based reach to grasp training after stroke

Pilot randomised controlled trial of home based reach to grasp training after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN56716589
Enrollment
60
Registered
2011-10-20
Start date
2011-11-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Stroke Research Network, rehabilitation - a community study Circulatory System Cerebrovascular disease, unspecified

Interventions

Reach to grasp training Task-specific training involves the practice of either whole or part movements, which are as much like the actual movement as possible. The exercises are graded according to th

Sponsors

University of the West of England (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A participant may enter the study if ALL of the following apply: 1. Diagnosis of stroke 2. Patient discharged home (i.e. permanent address, may include care home/sheltered accommodation) 3. Has remaining upper limb movement deficit defined as being unable to pick up a 6mm ball bearing from the table top, between index finger and thumb, and place it on a shelf 37 cm above table 4. Informed written consent Non-English speakers will be included with the aid of family or friends to translate. Aphasic patients will be included because the trial steering committee knows from previous clinical experience that task-specific training can be delivered to aphasic patients via the use of communication other than spoken language (e.g. gestures, strategic use of environmental cues).

Exclusion criteria

Exclusion criteria: A participant may not enter the study if ANY of the following apply: 1. Upper limb movement deficits attributable to non-stroke pathology 2. Unable to lift hand off lap when asked to place hand behind head 3. Severe fixed contractures of elbow or wrist (i.e. grade 4 on the modified Ashworth scale) 4. Shoulder pain 5. More than 12 months post-stroke

Design outcomes

Primary

MeasureTime frame
Action Research Arm Test measured 6 weeks after baseline assessment is primary time point.Assessed again at 3 and 6 months after baseline.

Secondary

MeasureTime frame
1. Motor Activity log measured 6 weeks after baseline and 3 & 6 months after baseline 2. Stroke Impact Scale measured 6 weeks after baseline and 3 & 6 months after baseline 3. Wolf Motor Function Test measured 6 weeks after baseline assessment and 3 & 6 months after baseline

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 23, 2026