Effectiveness of occupational therapy (OT) intervention with patients with early stage rheumatoid arthritis (RA)
| ISRCTN | ISRCTN46762597 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN46762597 |
| Secondary identifying numbers | H0598 |
- Submission date
- 15/07/2002
- Registration date
- 15/07/2002
- Last edited
- 05/01/2011
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Musculoskeletal Diseases
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Alison Hammond
Scientific
Scientific
Rheumatology
Derbyshire Royal Infirmary
London Road
Derby
DE1 2QY
United Kingdom
| Phone | +44 (0)1332 347141 |
|---|---|
| alison.hammond@sdah-tr.trent.nhs.uk |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Not specified |
| Study type | Not Specified |
| Scientific title | |
| Study acronym | ROTA |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Rheumatoid arthritis (RA) |
| Intervention | 1. Treatment group: Four x 1 h individual appointments, 2 h education programme, two x 1 h review appointments at 6 and 12 months. Individual assessment: Activities of daily living assessment and relevant training, provision of assistive devices; hand assessment plus training in joint protection, hand exercises and splint provision as necessary; relevant advice on work, leisure, information about RA and its management, foot care, upper and lower limb exercises, posture advice. Psychosocial support. 2. Control group: Usual rheumatology out-patient care (ie clinic appointments and referral to physiotherapy and occupational therapy if essential). |
| Intervention type | Other |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/01/2003 |
| Completion date | 31/12/2003 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | 1. Diagnosed with rheumatoid arthritis by a Consultant Rheumatologist within last 2.5 years 2. Willing to attend for regular appointments 3. Stable on medical treatment or about to enter the agreed North Thames Rheumatology Audit Group treatment protocol |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/2003 |
| Date of final enrolment | 31/12/2003 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Rheumatology
Derby
DE1 2QY
United Kingdom
DE1 2QY
United Kingdom
Sponsor information
Arthritis Research Campaign (ARC) (UK)
Charity
Charity
Copeman House
St Mary's Gate
Chesterfield
S41 7TD
United Kingdom
| Phone | +44 (0)300 790 0400 |
|---|---|
| enquiries@arthritisresearchuk.org | |
| Website | http://www.arc.org.uk |
"ROR" |
https://ror.org/02jkpm469 |
Funders
Funder type
Charity
Arthritis Research Campaign (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| 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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/01/2004 | Yes | No |
