Effects of Isometric Versus Isotonic Exercise in Female Patients With Osteoarthritis

Sponsor
Superior University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05873088
Collaborator
(none)
64
1
2
5
12.8

Study Details

Study Description

Brief Summary

to find out the Effects of Isometric Versus Isotonic Exercise in Female Patients With Osteoarthritis

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Isometric
  • Diagnostic Test: Isotonic Exercise
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Effects of Isometric Versus Isotonic Exercise in Female Patients With Osteoarthritis
Actual Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Isometric

Diagnostic Test: Isometric
Effects of Isometric Exercise in Female Patients With Osteoarthritis

Experimental: Isotonic Exercise

Diagnostic Test: Isotonic Exercise
Effects of Isotonic Exercise in Female Patients With Osteoarthritis

Outcome Measures

Primary Outcome Measures

  1. WOMAC Scale [6 Months]

    Isometric Versus Isotonic Exercise in Female Patients With Osteoarthritis by using WOMAC Scale

  2. VAS score [6 Months]

    Isometric Versus Isotonic Exercise in Female Patients With Osteoarthritis by using VAS score

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 60 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Female patients with osteoarthritis Age group of 35 to 60
Exclusion Criteria:
  • Patients admitted in ICU or HDU Patients with any mental illness

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chaudhary Muhammad Akram Hospital Lahore Punjab Pakistan

Sponsors and Collaborators

  • Superior University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Muhammad Naveed Babur, Principal Investigator, Superior University
ClinicalTrials.gov Identifier:
NCT05873088
Other Study ID Numbers:
  • DPT/Batch-Fall18/538
First Posted:
May 24, 2023
Last Update Posted:
May 24, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 24, 2023