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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02469025
Other study ID # PI13/0030
Secondary ID
Status Completed
Phase Phase 3
First received May 26, 2015
Last updated May 1, 2017
Start date January 2014
Est. completion date April 2017

Study information

Verified date May 2017
Source Universidad de Zaragoza
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 2017
Est. primary completion date May 2016
Accepts healthy volunteers No
Gender All
Age group 45 Years to 90 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Manual caudal traction mobilization in resting position

Manual caudal traction mobilization in end range position

Selftreatment
Each subject is advice to do some exercises at home

Locations

Country Name City State
Spain Unidad de Investigación en Fisioterapia. Universidad de Zaragoza Zaragoza

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Zaragoza

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline in Passive Hip Range of Motion after intervention, at 3 weeks post-intervention and at 6 weeks post intervention 3 weeks, 6 weeks, 9 weeks
Secondary 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 3 weeks, 6 weeks, 9 weeks
Secondary Change from Baseline in Pain on the Visual Analog Scale after intervention, at 3 weeks post-intervention and at 6 weeks post intervention 3 weeks, 6 weeks, 9 weeks
Secondary Change from Baseline in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scale after intervention and at 6 weeks post intervention 3 weeks, 9 weeks
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