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The effects of a combined lifestyle intervention in overweight patients with hip osteoarthritis: a pilot study

The effects of a combined lifestyle intervention in overweight patients with hip osteoarthritis: a pilot study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26093
Enrollment
25
Registered
2007-09-06
Start date
2007-10-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Obese, overweight, osteoarthritis of the hip, exercise, weight loss, lifestyle intervention, combination therapy, pain, functional abilities.

Interventions

The physical exercise therapy will be divided in an individual phase (2 to 3 months) and a group phase (3 months) (total of 6 months). Additionally the patients will be stimulated to get active, or s

Sponsors

Department of Orthopaedic Surgery University Medical Center Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients of 40 years and older with a calculated body mass index of 25 or more and radiographic and/or clinical evidence of hip osteoarthritis. The osteoarthritis presents with pain in combination with either (a) hip internal rotation equal or more than 15º, pain present on internal rotation of the hip, morning stiffness of the hip equal or less than 60 min or (b) hip internal rotation less than 15º, and hip flexion equal or less than 115º.

Exclusion criteria

Exclusion criteria: Patients with severe medical conditions that prevents safe participation in an exercise program (such as angina pectoris, peripheral vascular disease, stroke, congestive heart failure, chronic obstructive pulmonary disease, insulin-dependent diabetes, psychiatric disease, renal disease, renal disease, liver disease, active cancer other than skin cancer, anaemia); symptoms of feet or ankle which could interfere with exercise programs; in case of rheumatic arthritis; an inability to walk without a cane or other assistive device; participation in another research study; inability to finish the study or unlikely to be compliant to the opinion of the clinical staff, because of frailty, illness, co morbidity or other reasons. Additionally patients who are not able to fill in a questionnaire as a result of language problems or dementia will be excluded.

Design outcomes

Primary

MeasureTime frame
Self-reported physical function as measured by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) (Roorda et al., 2004).

Secondary

MeasureTime frame
Body weight; height, objective functional abilities measured with use of a walking test of 20 meters, and the Timed Up and Go test (de Greef et al 2006); Pain measured by the WOMAC physical function scale and the health related Quality of Life measured by the SF-36 (Aaronson et al., 1998). The SQUASH (Wendel-Vos e.a. 2003) will be used to get an impression of the physical activity pattern.

Contacts

Public ContactNienke Paans

Hanzeplein 1

n.paans@orth.umcg.nl++31 50 361 0568

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)