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Effect of Talar Mobilization With Movement Versus Acupuncture on Knee Pain and Function in the Postmenopausal Women

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ClinicalTrials.gov Identifier: NCT06051903
Recruitment Status : Not yet recruiting
First Posted : September 25, 2023
Last Update Posted : February 28, 2024
Sponsor:
Information provided by (Responsible Party):
Kerolous Ishak Shehata, October 6 University

Study Description
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Brief Summary:
The purpose of this study is to determine the effect of talar mobilization with movement versus acupuncture on knee pain and function in the postmenopausal women

Condition or disease Intervention/treatment Phase
Talar Mobilization Acupuncture Other: Mobilization wih movement Not Applicable

Detailed Description:
A sample of forty postmenopausal women were selected from Department of Gynecology and Obstetrics, Participants were assigned into two groups (group A) postmenopausal women who receive the talar mobilization with movement technique for knee joint , their age raged from 50-60 years (n= 20) and (group B) postmenopausal women who receive acupuncture for knee joint (n= 20), their age ranged from 50-60 years and body mass index (BMI) for both groups were less than 30 kg/m2. All participants were evaluated through measuring knee range of motion by using goniometer and the degree of knee pain by using numeric rating scale and pressure algometer
Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Effect of Talar Mobilization With Movement Versus Acupuncture on Knee Pain and Function in the Postmenopausal Women
Estimated Study Start Date : March 2024
Estimated Primary Completion Date : May 2024
Estimated Study Completion Date : June 2024

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Acupuncture

Arms and Interventions
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Arm Intervention/treatment
Experimental: Talar mobilization with movement
(group A) postmenopausal women who receive the talar mobilization with movement technique for knee joint , their age raged from 50-60 years (n= 20)
 Other: Mobilization wih movement
The purpose of this study is to determine the effect of talar mobilization with movement versus acupuncture on knee pain and function in the postmenopausal women
Experimental: Acupuncture for knee joint
(group B) postmenopausal women who receive acupuncture for knee joint (n= 20), their age ranged from 50-60 years
 Other: Mobilization wih movement
The purpose of this study is to determine the effect of talar mobilization with movement versus acupuncture on knee pain and function in the postmenopausal women


Outcome Measures
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Primary Outcome Measures :
  1. . Numeric pain rating scale [ Time Frame: up to 4 weeks ]
    it will measure pain intensity


Secondary Outcome Measures :
  1. KOOS questionnaire [ Time Frame: up to 4 weeks ]
    To measure success of range of motion

  2. Pressure algometer [ Time Frame: up to 4 weeks ]
    To measure the pain


Eligibility Criteria
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Ages Eligible for Study:   50 Years to 60 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   their age ranged from 50-60 years
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • ) Females patients refered from orthopedic surgeon diagnosed with knee OA (2) Their age ranged from 50 _60 years old 3) Their BMI less than 30 kg/m2. 5) knee pain in the previous week with an intensity of at least 3 points on a numeric pain rating scale (NPRS ) (5) Patients limited ankle dorsiflexion ROM 6) All Patients had 3 points on NPS (7) Presence of knee pain for at least 3 moonths 8) All patients were given the arabic version of KOOS questionnaire

Exclusion Criteria:

  • 1) Patients with Rheumatoid arthritis 2) Their BMI more than 30 kg/m2. 3) Unrelated to any traumatic knee event 4) Patients with Previous tibial fracture 5) Patients with Ankle instability 6) Patients with previous meniscal degeneration 7) Patients with hyper laxity 8) Patients with neurological disorders
Contacts and Locations
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Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06051903


Contacts
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Contact: Kerolous Kelini +201229712126 Kerolous.ishak.pt@o6u.edu.eg

Sponsors and Collaborators
October 6 University
More Information
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Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
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Responsible Party: Kerolous Ishak Shehata, principle investigator, October 6 University
ClinicalTrials.gov Identifier: NCT06051903    
Other Study ID Numbers: p.t.REC\012\004591
First Posted: September 25, 2023    Key Record Dates
Last Update Posted: February 28, 2024
Last Verified: February 2024

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No