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Increasing physical activity in older people with persistent musculoskeletal pain

The iPOPP study: a pragmatic, three-parallel-arm, individually randomised controlled trial with parallel health economic and process evaluation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN17816427
Enrollment
1086
Registered
2019-02-26
Start date
2019-06-04
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Persistent musculoskeltal pain Musculoskeletal Diseases

Interventions

Participants will be individually randomised to one of the three arms of the study (allocation 1:1:1 ratio), using random permuted blocks, stratified by general practice. Usual primary care: Partici

Sponsors

Keele University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 65 years and over 2. Consulted at general practice for musculoskeletal pain in one or more index sites (foot, knee, hip, back, shoulder, neck) in the last 12 months 3. Registered with one of the participating GP practices during the specified trial period for that practice 4. Pain that has lasted for > 3 months and a current Chronic Pain Grade (Von Korff et al., 1992) score of between 2 to 4, determined through a brief postal chronic pain screening survey

Exclusion criteria

Exclusion criteria: 1. Patients with complex medical conditions deemed at risk of walking-related complications (e.g. new onset chest pain (within the last 3 months, chest pain on exercise, severe hypertension, syncope (within the last 12 months), recent lower limb fracture (within the last three months), active and severe synovitis 2. Vulnerable patients (i.e. patients with significant cognitive impairment (e.g. dementia; psychotic illness), or in palliative stage of care) 3. Patients who reside in a residential or nursing homes 4. Unable to provide full, informed, written consent

Design outcomes

Primary

MeasureTime frame
Average daily step count per day over 7 days measured via accelerometry on four occasions (baseline, 3, 6 and 12 months post randomisation)

Secondary

MeasureTime frame
Measured at baseline, 3, 6 and at least 12 months follow up, except where specified differently: 1. Pain intensity and location, measured using the Numeric Pain Intensity Scale, pain manikin 2. Physical function, measured using the PF-10 from the SF-36 3. Physical activity, measured using IPAQ-E 4. Sedentary time, measured using accelerometry 5. Health-related quality of life, measured using EQ-5D-5L 6. Non-health aspects of quality of life, measured using ICECAP-O 7. Self-efficacy, measured using Self-Efficacy for Exercise Scale 8. Anxiety, measured using GAD-7 9. Depression, measured using PHQ 8 10. Healthcare resource use, measured using patient self -reported questionnaires at 6 and 12 months follow-up 11. Adverse events, measured using patient self -reported questionnaires at 3,6 and 12 months follow-up 12. Pedometer use, measured using patient self -reported questionnaires at 3,6 and 12 months follow-up 13. Consultation experience (iPOPP intervention only), measured using patient self -reported questionnaires at 3 month follow-up

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026