The role of pressure feedback in muscle patterning shoulder instability
ISRCTN | ISRCTN65243663 |
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DOI | https://doi.org/10.1186/ISRCTN65243663 |
Secondary identifying numbers | N0209167764 |
- Submission date
- 29/09/2006
- Registration date
- 29/09/2006
- Last edited
- 17/07/2009
- Recruitment status
- Stopped
- Overall study status
- Stopped
- Condition category
- Musculoskeletal Diseases
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Miss Anju Jaggi
Scientific
Scientific
Royal National Orthopaedic Hospital
Brockley Hill
Stanmore
HA7 4LP
United Kingdom
Study information
Study design | Randomised controlled trial |
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Primary study design | Interventional |
Secondary study design | Randomised controlled trial |
Study setting(s) | Not specified |
Study type | Treatment |
Scientific title | |
Study objectives | Does the application of Tubigrip on the symptomatic arm affect grip strength, dexterity and shoulder movement in patients with muscle patterning instability? |
Ethics approval(s) | Not provided at time of registration |
Health condition(s) or problem(s) studied | Musculoskeletal Diseases: Shoulder disorders |
Intervention | Participants will have their grip strength assessed, and dexterity measured via the 9-hole peg test. They will then be randomised to receive treatment (Tubigrip) or nothing, and asked to rest for 30 minutes. Following a 30-min rest, they will be asked to repeat these tests in front of a second assessor, who is blinded to whether they have received the treatment or not. Both groups will be asked to keep a symptom diary for 14 days. Added 17/07/09: trial stopped due to lack of resources and change in objectives. |
Intervention type | Other |
Primary outcome measure | Active range of shoulder movement, grip strength, dexterity, subjective improvement rating by patient. |
Secondary outcome measures | Not provided at time of registration |
Overall study start date | 18/08/2005 |
Completion date | 10/01/2006 |
Reason abandoned (if study stopped) | Lack of staff/facilities/resources + Objectives no longer viable |
Eligibility
Participant type(s) | Patient |
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Age group | Adult |
Sex | Not Specified |
Target number of participants | 70 |
Key inclusion criteria | 70 patients with symptoms of shoulder instability and/or pain and have a suspicion or diagnosis of muscle patterning abnormality. |
Key exclusion criteria | Not provided at time of registration |
Date of first enrolment | 18/08/2005 |
Date of final enrolment | 10/01/2006 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Royal National Orthopaedic Hospital
Stanmore
HA7 4LP
United Kingdom
HA7 4LP
United Kingdom
Sponsor information
Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Government
Government
The Department of Health, Richmond House, 79 Whitehall
London
SW1A 2NL
United Kingdom
Phone | +44 (0)20 7307 2622 |
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dhmail@doh.gsi.org.uk | |
Website | http://www.dh.gov.uk/Home/fs/en |
Funders
Funder type
Government
Royal National Orthopaedic Hospital NHS Trust (UK), NHS R&D Support Funding
No information available
Results and Publications
Intention to publish date | |
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Individual participant data (IPD) Intention to share | No |
IPD sharing plan summary | Not provided at time of registration |
Publication and dissemination plan | Not provided at time of registration |
IPD sharing plan |