Hip Osteoarthritis Clinical Trial
— HipOAOfficial title:
Assessment and Treatment Responses to Patient Education and Basic Body Awareness Therapy in Hip Osteoarthritis: a Randomized Controlled Trial
Verified date | October 2019 |
Source | University of Bergen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The incidence of hip osteoarthritis (OA) is rising in western countries due to an ageing population and the epidemic of obesity. Patients with hip OA tend to complain of hip pain and stiffness which affect alignment and mobility of the whole body and typically result in general musculoskeletal pain and disability. Clinical guidelines recommend a combination of exercise therapy, weight loss and education, adjusted to the individuals needs, to be tried out before arthroplasty eventually is offered. However, to obtain a satisfactory long-term outcome is a challenge as patients may not be motivated to comply with a training program including functional strength and mobility training, if not guided by a therapist. Basic Body Awareness Therapy (BBAT) may be an alternative training modality with a better potential for lasting effects. It is a low-impact movement therapy focusing on alignment of the body and quality of movements, implemented in daily life activities. In the BBAT learning process by doing, reflecting on and transferring body awareness into daily life movements, the investigators hypothesize that the patients will obtain self-efficacy and mastering, of importance for continued training on their own. This hypothesis will be examined in the present randomized controlled trial, comparing Patient Education combined with BBAT and Patient Education alone. The investigators will, accordingly, examine the supplementary effects of BBAT for patients with hip OA. They will also explore the importance of movement quality as observed by physiotherapist using Body Awareness Rating Scale, and how it relates to how patients perceive their movement performance. In the study the investigators will particularly address long-term effects of the intervention by comparing survival of the native hip in the two groups included in the study. Data from the study will be included in a national database of patients with non-surgical treatment of hip and knee OA (NOAR), giving rise to comparison of different movement therapies.
Status | Completed |
Enrollment | 101 |
Est. completion date | January 2019 |
Est. primary completion date | January 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Women and men with primary OA according to the American College of Rheumatology Clinical Criteria, living in Bergen or within a reasonable travelling distance (judged by the patients). Exclusion Criteria: - Other known major physical or mental problems or disease that precludes movement training and participation in an educational program, known drug abuse, not speaking or understanding Norwegian language, pregnancy 5-9 months. |
Country | Name | City | State |
---|---|---|---|
Norway | University of Bergen | Bergen |
Lead Sponsor | Collaborator |
---|---|
University of Bergen | Bergen University College, Haukeland University Hospital |
Norway,
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* Note: There are 57 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Numeric Rating Scale, change in pain | Pain intensity during walking | Baseline, 4 months and 1 year | |
Primary | Hip disability and Osteoarthritis Outcome Score (HOOS), change in ADL | Self-reported disability | Baseline, 4 months and 1 year | |
Secondary | Harris Hip Score (HHS) | Assesses hip disabilities and effect of treatment on four domains | Baseline, 4 months and 1 year | |
Secondary | The EuroQol (EQ-5D-5L) | A generic health index comprising a five-part questionnaire and a visual analogue self-rating scale | Baseline, 4 months and 1 year | |
Secondary | Arthritis Self-efficacy Scale (ASES) | A questionnaire about self-efficacy regarding pain and symptoms | Baseline, 4 months and 1 year | |
Secondary | The Patient Global Impression of Change (PGIC) | Assesses the patients' own impression of change over time | 4 months and 1 year | |
Secondary | 6-minutes walking - test | Walking distance (inside) during the time limit of 6 minutes | Baseline, 4 months | |
Secondary | Chair test. | The patient repeats rising up from a chair and sitting down during 30 seconds and the number is counted | Baseline, 4 months | |
Secondary | Stairs test. | The number of seconds used to walk up and down 18 steps x 3 is measured | Baseline, 4 months | |
Secondary | Body Awareness Rating Scale (BARS) | Consists of two assessment parts: 1) observation and assessment of movement quality based on 12 movements and 2) interview with the patient about movement awareness immediately after exploring each movement. | Baseline, 4 months | |
Secondary | UCLA Activity Score | Assesses degree of Activity on ordinal scale | Baseline, 4 months and 1 year |
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