- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00808483
Walking Skill Training Program Effects in Patients With Total Hip Arthroplasty
January 8, 2015 updated by: Kristi E Heiberg, PhD, University of Oslo
Effect of a Walking Skill Training Program in Patients Who Have Undergone Total Hip Arthroplasty: Followup One Year After Surgery
Rehabilitation plays an important part after total hip arthroplasty. In this common practice few studies have been performed on this issue.
The aims of this study were:
- to examine the immediate effects of a walking skill training program on walking, stair climbing, balance, self-reported physical functioning physical functioning, pain and self-efficacy compared to a control group without supervised physiotherapy
- to examine whether the effects persisted 12 months after surgery
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
68
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Oslo 0317
-
Oslo, Oslo 0317, Norway, 1089 Blindern
- Department of health science, University of Oslo
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
45 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Primary cox arthrosis
- Good written and oral Norwegian language
Exclusion Criteria:
- Severe hip arthrosis in the other hip or severe gon arthrosis that restricted walking
- Neurological disorders
- Rheumatoid arthritis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Walking skill training group
Participation in the supervised walking skill training program.
|
12 individualized training sessions containing functional exercises like walking, stair climbing, balance training and with supervision and guidance from a physiotherapist.
|
|
No Intervention: Control group
No participation in the supervised walking skill training program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
6 Minutes Walk Test (6MWT)
Time Frame: 5 months and 12 months
|
Participants walked in a 40 meter hospital corridor for 6 minutes.
|
5 months and 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hip Dysfunction and Osteoarthritis Outcome Score (HOOS)
Time Frame: 5 months and 12 months
|
Self-reported symptoms, pain, physical function, function in sport and recreation, quality of life.
0 (worse) - 100 (best)
|
5 months and 12 months
|
|
Harris Hip Score (HHS)
Time Frame: 5 months and 12 months
|
Pain and physical function.
0 (worse) - 100 (best)
|
5 months and 12 months
|
|
Self-efficacy
Time Frame: 5 months and 12 months
|
Self-reported self-efficacy in activities.
0 (worse) - 100 (best).
|
5 months and 12 months
|
|
Stair Climbing Test (ST)
Time Frame: 5 months and 12 months
|
Ascend and descend 8 steps with a step hight of 16 cm as fast as they could without running.
Few seconds (best) - many seconds (worse)
|
5 months and 12 months
|
|
ROM Extension
Time Frame: 5 months and 12 months
|
Active range of motion (ROM) in hip extension test.
Degrees is registered.
0 degrees indicates zero position of the hip, minus digrees indicates flexion contracture.
|
5 months and 12 months
|
|
Index of Muscle Function (IMF)
Time Frame: 5 months and 12 months
|
Tests of general mobility, muscle strength, balance/coordination, and endurance.
40 (worse) - 0 (best)
|
5 months and 12 months
|
|
Figure-of-eight Test
Time Frame: 5 months and 12 months
|
Test of dynamic balance.
Number of steps on and outside the line is registered.
0 (best)
|
5 months and 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kristi E Heiberg, PhD, University of Oslo
- Principal Investigator: Kristi E Heiberg, PhD, Bærum Hospital Vestre Viken
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2008
Primary Completion (Actual)
April 1, 2011
Study Completion (Actual)
April 1, 2011
Study Registration Dates
First Submitted
December 12, 2008
First Submitted That Met QC Criteria
December 12, 2008
First Posted (Estimate)
December 15, 2008
Study Record Updates
Last Update Posted (Estimate)
January 9, 2015
Last Update Submitted That Met QC Criteria
January 8, 2015
Last Verified
January 1, 2015
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2008/2325
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.