The role of pressure feedback in muscle patterning shoulder instability
| ISRCTN | ISRCTN65243663 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN65243663 |
| Protocol serial number | N0209167764 |
| Sponsor | Record Provided by the NHSTCT Register - 2006 Update - Department of Health |
| Funder | Royal National Orthopaedic Hospital NHS Trust (UK), NHS R&D Support Funding |
- 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
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| 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(s) |
Active range of shoulder movement, grip strength, dexterity, subjective improvement rating by patient. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 10/01/2006 |
| Reason abandoned (if study stopped) | Lack of staff/facilities/resources + Objectives no longer viable |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Not Specified |
| Target sample size at registration | 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
- United Kingdom
- England
Study participating centre
Royal National Orthopaedic Hospital
Stanmore
HA7 4LP
United Kingdom
HA7 4LP
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |