The purpose of the study is to evaluate the effect of manual treatment and a patient education programme for patients without indication for hip surgery.
Hip osteoarthritis (hip OA) is the second most common arthritis of the larger joints and may result in pain and disability and lead to reduced quality of life (QoL). The prevalence of hip OA, in the adult population, \> 35 years, is estimated to 4-11% in the western society. In specific countries hip OA affects up to 25% in adults \> 60 years. With a growing elder population, these prevalence rates will increase and the demand for cost-effective and safe interventions will increase as well. International guidelines, 2008, on the management of hip and knee OA recommend a combination of non-pharmacological and pharmacological treatment. For years the majority of interventional research for hip and knee OA has focused on surgery and drugs. Surgery is an option, when pain and disability have reached severe levels, and an increasing group of patients are today looking for other treatment options than drug treatment (pharmacological). In the last 4-6 years, new randomized controlled trials (RCT) have shown promising results with non-pharmacological treatment, such as exercise, patient education, manual therapy and acupuncture. The purpose of this RCT is to investigate the effect of combining manual treatment and a patient education programme and compare it to a minimal intervention in form of a home stretching programme. It will further investigate the specific effect of manual treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
118
The hip school consists of one initial personal interview, three group sessions, and one follow-up personal interview. The hip school is a patient education programme which involves anatomy/physiology, epidemiology, disease progression and pain, advice on self-help and exercises.
Hip school as above. Patients receive manual treatment twice a week for 6 weeks. Manual treatment consists of joint manipulation and muscle energy techniques to the articular and soft-tissue structures of the hip.
As control group, an information leaflet is used with instructions to live as usual during the 6 weeks intervention period. The exercise sheet of the hip school is given to the patients with no further instruction.
Department of Ortopaedic Surgery and Traumatology, Odense University Hospital
Odense, DK, Denmark
Pain: Numerical pain scale
Time frame: Baseline, 6 weeks, 3 months, 1 year
Hip Disability and Osteoarthritis Outcome Score
Time frame: Baseline, 6 weeks, 3 months, 1 year
General improvement experienced by patient - "Global Assessment"
Time frame: Baseline, 6 weeks, 3 months, 1 year
Quality of life: EQ-5D
Time frame: Baseline, 6 weeks, 3 months, 1 year
Passive hip range of motion
Time frame: Baseline, 6 weeks, 3 months, 1 year
Hip surgery up to one year after baseline
Time frame: Baseline, 6 weeks, 3 months, 1 year
Use of pain medication
Time frame: Baseline, 6 weeks, 3 months, 1 year
Patient Specific Hip Disability
Time frame: Baseline, 6 weeks, 3 months, 1 year
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