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Maintained physical activity and physiotherapy in the management of distal arm pain

Maintained physical activity and physiotherapy in the management of distal arm pain: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN79085082
Enrollment
555
Registered
2012-02-17
Start date
2012-01-30
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Distal arm pain Musculoskeletal Diseases Pain in limb

Interventions

Advice to remain active: Participants randomised to receive advice to remain active will receive a leaflet focusing on shifting beliefs about activity, and including practical advice.

Sponsors

University of Aberdeen (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Entry on to out-patient physiotherapy waiting list for treatment for distal arm pain / disability following self-referral or referral from primary care and 2. Aged =18 years at the time of screening

Exclusion criteria

Exclusion criteria: 1. Previous physiotherapy for distal arm pain (within the past 12 months) 2. Pain for which physiotherapy of the distal arm is not the primary treatment (e.g. referred pain from the neck / shoulder) 3. Arm pain arising from fracture or systemic inflammatory disease 4. Pain arising from cancer 5. Complex Regional Pain Syndrome (CRPS) 6. Specific condition for which advice to remain active is contraindicated (e.g. evidence of florid tenosynovitis) 7. Classed as an emergency appointment 8. Embroiled in legal dispute regarding arm pain

Design outcomes

Primary

MeasureTime frame
The proportion of patients free of disability at 26 weeks post-randomisation, as determined by the modified - Disabilities of the Arm, Shoulder and Hand (DASH)

Secondary

MeasureTime frame
1. Determine the proportion of participants who still seek physiotherapy at 6 weeks 2. Collect information on the type of treatments given, and time to discharge 3. Arm pain and function 4. Coping 5. Fear of movement 6. Ability to function at work 7. Aspects of general health and quality of life Measured at 6, 13, and 26 weeks post-randomisation by self complete postal questionnaire using validated instruments

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 21, 2026