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Clinical Trials/NL-OMON26093
NL-OMON26093
Recruiting
Not Applicable

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

Department of Orthopaedic Surgery University Medical Center Groningen0 sites25 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obese, overweight, osteoarthritis of the hip, exercise, weight loss, lifestyle intervention, combination therapy, pain, functional abilities.
Sponsor
Department of Orthopaedic Surgery University Medical Center Groningen
Enrollment
25
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Department of Orthopaedic Surgery University Medical Center Groningen

Eligibility 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

  • 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.

Outcomes

Primary Outcomes

Not specified

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