- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02469025
Effects of Grade III Traction-mobilization in End-range Joint Position in Patients With Hip Osteoarthritis
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Phase 3
Contacts and Locations
Study Locations
-
-
-
Zaragoza, Spain, 50009
- Unidad de Investigación en Fisioterapia. Universidad de Zaragoza
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Hip osteoarthritis diagnosis
- Diminished range of motion
- Sign the informed consent
Exclusion Criteria:
- Contraindications to Manual Therapy.
- Sensitivity impairments in low back, pelvis, knee or foot regions.
- Being involved in other physical therapy treatments
- To change medication use during the study
Study Plan
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: Resting position mobilization group
This group receive six manual therapy interventions based on manual traction mobilization in a resting position of the hip joint. In addition the physical therapist teach the patients six exercises to do at home between manual mobilization sessions. |
Each subject is advice to do some exercises at home
|
|
Experimental: End range position mobilization group
This group receive six manual therapy interventions based on manual traction mobilization in an end range position of the hip joint. In addition the physical therapist teach the patients six exercises to do at home between manual mobilization sessions. |
Each subject is advice to do some exercises at home
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change from Baseline in Passive Hip Range of Motion after intervention, at 3 weeks post-intervention and at 6 weeks post intervention
Time Frame: 3 weeks, 6 weeks, 9 weeks
|
3 weeks, 6 weeks, 9 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Changes from Baseline in Functional Tests (TUG, fast-paced walk test, stair climb test, 30sec. chair stand test), after intervention, at 3 weeks post-intervention and at 6 weeks post intervention
Time Frame: 3 weeks, 6 weeks, 9 weeks
|
3 weeks, 6 weeks, 9 weeks
|
|
Change from Baseline in Pain on the Visual Analog Scale after intervention, at 3 weeks post-intervention and at 6 weeks post intervention
Time Frame: 3 weeks, 6 weeks, 9 weeks
|
3 weeks, 6 weeks, 9 weeks
|
|
Change from Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scale after intervention and at 6 weeks post intervention
Time Frame: 3 weeks, 9 weeks
|
3 weeks, 9 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PI13/0030
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.
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