Benefits of Effective Exercise for knee Pain - The BEEP main trial

Conditions

Musculoskeletal, All Diseases Musculoskeletal Diseases Pain in joint: knee

McKevitt S, Healey E, Jinks C, Rathod-Mistry T, Quicke J.

2020-06-0121 citations

10.1016/j.ocarto.2020.100057

Optimal primary care management of clinical osteoarthritis and joint pain in older people: a mixed-methods programme of systematic reviews, observational and qualitative studies, and randomised controlled trials

Elaine M. Hay, Krysia Dziedzic, Nadine E. Foster, George Peat, Daniëlle van der Windt et al. (25 authors)

Programme Grants for Applied Research2018-07-0121 citations

10.3310/pgfar06040

Change in physical activity level and clinical outcomes in older adults with knee pain: a secondary analysis from a randomised controlled trial.

Quicke JG, Foster NE, Croft PR, Ogollah RO, Holden MA.

2018-02-1712 citations

10.1186/s12891-018-1968-z

A multicentre, pragmatic, parallel group, randomised controlled trial to compare the clinical and cost-effectiveness of three physiotherapy-led exercise interventions for knee osteoarthritis in older adults: the BEEP trial protocol (ISRCTN: 93634563).

Foster NE, Healey EL, Holden MA, Nicholls E, Whitehurst DG, Jowett S, Jinks C, Roddy E, Hay EM, BEEP trial team.

2014-07-2733 citations

10.1186/1471-2474-15-254

Interventions

Individually Tailored Exercise Patients will receive between 6-8 face-to-face treatment sessions with a physiotherapist within 12 weeks Targeted Exercise Adherence Gro

Study Entry : Registration and One or More Randomisations

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Aged 45 years and over 2. Knee pain or stiffness in one or both knees 3. Primary care consulters willing to particpate in the study 4. Able to give informed consent 5. Has access to telephone 6. Able to read and write in English 7. Target Gender: Male & Female

Exclusion criteria

Exclusion criteria: 1. Those with potentially serious pathology 2. Those on a waiting list to have a hip or knee replacement to affected side 3. Those who have already had a hip or knee replacement to affected side 4. When the knee problem is caused by a recent sports injury, fall or accident 5. Those for whom exercise interventions are contra-indicated 6. Those who have had an exercise programme from a physiotherapist, or an injection in the last 3 months 7. Those living in a nursing home

Design outcomes

Primary

Measure	Time frame
Pain and Function from the WOMAC (Western Ontario and McMaster Universities) Index of Osteoarthritis WOMAC is collected at baseline, 3, 6, 9, 18 and 36 months	—

Secondary

Measure	Time frame
1. 7-day accelerometry; Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 2. Anxiety (GAD-7); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 3. Body Mass Index; Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 4. Cost-effectiveness; Timepoint(s): Collected at 3, 6, 9, 18 and 36 months 5. Depression (PHG-8); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 6. Exercise adherence; Timepoint(s): Collected at 3, 6, 9, 18 and 36 months 7. Healthcare utilisation (self report & Med Rec Review); Timepoint(s): Collected at 6, 18 and 36 months 8. ICE CAP-A capabilities; Timepoint(s): Collected at baseline, 6 and 18 months 9. Illness Perceptions (IPQ); Timepoint(s): Collected at baseline, 3 and 6 months 10. Medication usage; Timepoint(s): Collected at baseline, 3, 6, 9, 18 months 11. OMERACT-OARSI; Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 12. Overall health status (EQ-SD); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 13. Patient's Global Assessment of Change; Timepoint(s): Collected at 3, 6, 9, 18 and 36 months 14. Physical activity levels (self report PASE); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 15. Self-efficacy for exercise (SEE); Timepoint(s): Collected at baseline, 3 and 6 months	—

Measure

Time frame

1. 7-day accelerometry; Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 2. Anxiety (GAD-7); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 3. Body Mass Index; Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 4. Cost-effectiveness; Timepoint(s): Collected at 3, 6, 9, 18 and 36 months 5. Depression (PHG-8); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 6. Exercise adherence; Timepoint(s): Collected at 3, 6, 9, 18 and 36 months 7. Healthcare utilisation (self report & Med Rec Review); Timepoint(s): Collected at 6, 18 and 36 months 8. ICE CAP-A capabilities; Timepoint(s): Collected at baseline, 6 and 18 months 9. Illness Perceptions (IPQ); Timepoint(s): Collected at baseline, 3 and 6 months 10. Medication usage; Timepoint(s): Collected at baseline, 3, 6, 9, 18 months 11. OMERACT-OARSI; Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 12. Overall health status (EQ-SD); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 13. Patient's Global Assessment of Change; Timepoint(s): Collected at 3, 6, 9, 18 and 36 months 14. Physical activity levels (self report PASE); Timepoint(s): Collected at baseline, 3, 6, 9, 18 and 36 months 15. Self-efficacy for exercise (SEE); Timepoint(s): Collected at baseline, 3 and 6 months

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Countries

United Kingdom

Outcome results

None listed