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NCT02125968 Clinical Trial

Therapeutic Effects of Video Game Play Therapy on Patients With Chronic Low Back Pain

Chronic Low Back Pain Clinical Trial

Official title:
Therapeutic Effects of Video Game Play Therapy on Patients With Chronic Low Back Pain:Randomized-Controlled Clinical Trail

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02125968
Other study ID # SKH-8302-103-DR-36
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date May 2014
Est. completion date December 2014

Study information
Verified date August 2023
Source Taipei Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the video game play therapy in patients with chronic low back pain.

Description:

Understanding the short- and medium-term therapeutic effects of video game play therapy for patients with chronic low back pain.

Recruitment information / eligibility
Status Terminated
Enrollment 70
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender All
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria: - chronic low back pain Exclusion Criteria: 1. low back pain accompanied by specific pathological conditions, such as infection, inflammation, fracture, or tumor 2. history of low back surgery with an implant 3. pregnancy of plans to become pregnant during the course of study 4. having received concurrent treatment for low back pain followed by another health care professional

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• interactive video game
short- and medium-term therapeutic effects
• therapeutic exercise
short- and medium-term therapeutic effects

Locations
Country Name City State
Taiwan Shin Kong Wu Ho-Su Memorial Hospital Taipie

Sponsors (2)
Lead Sponsor Collaborator
Taipei Medical University Shin Kong Wu Ho-Su Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Oswestry Disability Questionnaire changes from baseline at one and three months after treatment
Secondary range of motion changes from baseline at one and three months after treatment
Secondary Hospital Anxiety and Depression Scale changes from baseline at one and three months after treatment
Secondary postural stability postural stability, limits of stability, and fall risk measured by Biodex Stability System changes from baseline at one and three months after treatment
Secondary Fear avoidance Behavior Questionnaire changes from baseline at one and three months after treatment
Secondary physical activity timed stairs climbing, 10-m walking, chair-rising time changes from baseline at one and three months after treatment
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