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Clinical Trials/NCT06051903
NCT06051903
Completed
Not Applicable

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

October 6 University1 site in 1 country40 target enrollmentMay 5, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Talar Mobilization Acupuncture
Sponsor
October 6 University
Enrollment
40
Locations
1
Primary Endpoint
. Numeric pain rating scale
Status
Completed
Last Updated
last year

Overview

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

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

Registry
clinicaltrials.gov
Start Date
May 5, 2023
End Date
April 22, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kerolous Ishak Shehata

principle investigator

October 6 University

Eligibility 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/m
  • 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

  • Patients with Rheumatoid arthritis 2) Their BMI more than 30 kg/m
  • 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

Outcomes

Primary Outcomes

. Numeric pain rating scale

Time Frame: up to 4 weeks

it will measure pain intensity

Secondary Outcomes

  • Pressure algometer(up to 4 weeks)
  • KOOS questionnaire(up to 4 weeks)

Study Sites (1)

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