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Effects of Grade III Traction-mobilization in End-range Joint Position in Patients With Hip Osteoarthritis

Primary Purpose

Osteoarthritis, Hip

Status
Completed
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Manual caudal traction mobilization in resting position
Manual caudal traction mobilization in end range position
Selftreatment
Sponsored by
Universidad de Zaragoza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Hip

Eligibility Criteria

45 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Unidad de Investigación en Fisioterapia. Universidad de Zaragoza

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Resting position mobilization group

End range position mobilization group

Arm Description

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.

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.

Outcomes

Primary Outcome Measures

Change from Baseline in Passive Hip Range of Motion after intervention, at 3 weeks post-intervention and at 6 weeks post intervention

Secondary Outcome Measures

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
Change from Baseline in Pain on the Visual Analog Scale after intervention, at 3 weeks post-intervention and at 6 weeks post intervention
Change from Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scale after intervention and at 6 weeks post intervention

Full Information

First Posted
May 26, 2015
Last Updated
May 1, 2017
Sponsor
Universidad de Zaragoza
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1. Study Identification

Unique Protocol Identification Number
NCT02469025
Brief Title
Effects of Grade III Traction-mobilization in End-range Joint Position in Patients With Hip Osteoarthritis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
April 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de Zaragoza

4. Oversight

5. Study Description

Brief Summary
Lower limb osteoarthritis is a major health problem in the westernized countries. The current gold standard treatment is joint replacement. However clinical guidelines recommend physical therapy as first option for these patients. Manual therapy has reported good reports in function, range of motion and pain in patients with hip osteoarthritis. The main aim of this study is to test the effects of a manual therapy protocol based on manual traction mobilization of the hip joint in an end range position and compare them with the effects achieve with the same protocol based on manual traction mobilization of the hip joint in a resting position. The investigators will use the caudal traction mobilization described by Kaltenborn. The study will test the effects of both treatments in passive range of motion, function and pain after three weeks of treatment, three weeks after finalizing the treatment and six weeks after.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Hip

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Resting position mobilization group
Arm Type
Experimental
Arm Description
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.
Arm Title
End range position mobilization group
Arm Type
Experimental
Arm Description
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.
Intervention Type
Other
Intervention Name(s)
Manual caudal traction mobilization in resting position
Intervention Type
Other
Intervention Name(s)
Manual caudal traction mobilization in end range position
Intervention Type
Other
Intervention Name(s)
Selftreatment
Intervention Description
Each subject is advice to do some exercises at home
Primary Outcome Measure Information:
Title
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
Secondary Outcome Measure Information:
Title
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
Title
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
Title
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

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Unidad de Investigación en Fisioterapia. Universidad de Zaragoza
City
Zaragoza
ZIP/Postal Code
50009
Country
Spain

12. IPD Sharing Statement

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Effects of Grade III Traction-mobilization in End-range Joint Position in Patients With Hip Osteoarthritis

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