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Effect of Exercise as Non-surgical Treatments on Time to Total Hip Replacement Surgery

NCT01697241 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2018-05-11

No results posted yet for this study

Summary

The aim of this trial is to test the hypothesis that patients with severe hip osteoarthritis postpone time to hip replacement surgery following participation in a patient education and supervised exercise program when compared to patients receiving patient education alone.

Conditions

Interventions

OTHER

Supervised exercise

Patients in the exercise groups will receive two types of exercise, delivered on separate days. One type of exercise is individualized, goal-based neuromuscular training (NEMEX-TJR) in groups with progression guided by the patient's neuromuscular function. The other type of exercise is individualized, intensive resistance training (RT) in groups with each exercise progression guided by load. Each of the two types of exercise will be offered weekly during the 12 week intervention period in sessions lasting 60-70 minutes. Thus, the entire exercise intervention consists of 24 sessions

OTHER

Patient education

The patient education program is designed to educate the patients about hip osteoarthritis during 3 sessions of 90 min. duration

Sponsors & Collaborators

  • Odense University Hospital

    collaborator OTHER

  • Institute for Clinical Research, Denmark

    collaborator INDUSTRY

  • Vejle Hospital

    collaborator OTHER

  • Region of Southern Denmark

    collaborator OTHER

  • The Danish Rheumatism Association

    collaborator OTHER

  • University of Southern Denmark

    lead OTHER

Principal Investigators

  • Carsten Jensen, PhD · Orthopedic Research Unit, Dept. of Orthopedic Surgery and Traumatology, Odense University Hospital, Denmark. Institute of Clinical Research, University of Southern Denmark, Denmark

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2017-08-31
Completion
2017-08-31

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01697241 on ClinicalTrials.gov