Comparison of the Accuracy in Rehabilitation Exercise Between Mobile Application Actuated Rehabilitation Exercise Guidance and Routine Rehabilitation Exercise Guidance for the Primary Osteoarthritis Knee Patients

March 2, 2020 updated by: Satit Thiengwittayaporn, Navamindradhiraj University

Comparison of the Accuracy in Rehabilitation Exercise Between Mobile Application Actuated Rehabilitation Exercise Guidance and Routine Rehabilitation Exercise Guidance for the Primary Osteoarthritis Knee Patients : A Randomized Controlled Trial

Evaluate the accuracy of physical therapy in various positions after 4 weeks of training, comparison of the accuracy in rehabilitation exercise between mobile application actuated rehabilitation exercise guidance and routine rehabilitation exercise guidance for the primary osteoarthritis knee patients

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Thailand
    • Bangkok
      • Dusit, Bangkok, Thailand, 10300
        • Navamindradhiraj University
    • Bangkok,
      • Dusit, Bangkok,, Thailand, 10300
        • Navamindradhiraj University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Primary osteoarthritis of knee
  • Have an android phone and use the application

Exclusion Criteria:

  • There are other complications that may affect physiotherapy
  • Communication problems
  • Has been trained in physical therapy for osteoarthritis patients
  • Have had total knee arthroplasty

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: mobile application actuated rehabilitation exercise guidance
Other: mobile application actuated rehabilitation exercise guidance
Mobile applications (also known as mobile apps) are software programs developed for mobile devices such as smartphones and tablets, to teach full function following injury and involves restoring strength, flexibility, endurance, and power.
Active Comparator: routine rehabilitation exercise guidance
Other: routine rehabilitation exercise guidance
the teach to practice full function following injury and involves restoring strength, flexibility, endurance, and power. It is achieved through various exercises and drills

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Outcome measurement to compare the accuracy
Time Frame: 1 month
To measurement by number of patient performing correct exercise has 3 exercise 10 steps and number of patient performing incorrect exercise has 3 exercise 10 steps. to compare the accuracy when osteoarthritis knee patients do rehabilitation using mobile application actuated rehabilitation exercise guidance and routine rehabilitation exercise guidance.If the patient is able to perform at least 8 times (80%), the patient will be define as corrected physical therapy, We compare the correction of physical therapy between the groups.
1 month
Patient satisfaction of rehabilitation method
Time Frame: 1 month

To compare the satisfaction of rehabilitation method after rehabilitation program of physical therapy by questionnaire. The satisfaction score has 5 point.

The 1 point mean the least satisfaction of patient to the method. The 2 point mean the less satisfaction of patient to the method. The 3 point mean the moderate satisfaction of patient to the method. The 4 point mean the much satisfaction of patient to the method. The 5 point mean the most satisfaction of patient to the method.
1 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Navamindradhiraj University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 4, 2018

Primary Completion (Actual)

September 1, 2019

Study Completion (Actual)

December 2, 2019

Study Registration Dates

First Submitted

September 3, 2018

First Submitted That Met QC Criteria

September 10, 2018

First Posted (Actual)

September 12, 2018

Study Record Updates

Last Update Posted (Actual)

March 3, 2020

Last Update Submitted That Met QC Criteria

March 2, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • COA 034/2561

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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