The Effect of Virtual Reality Exercises on Patients With Post-COVID-19 Condition
Effect of Motion-Controlled Video Games-Based Virtual Reality Exercise On Pain, Fatigue, Mood, Functional Capacity, And Quality of Life in Patients With Post-Covid-19 Condition: A Randomized Controlled Trial
1 other identifier
interventional
79
1 country
1
Brief Summary
This study aims to investigate (I) the effectiveness of motion-controlled video game-based VR exercises on pain, fatigue, functional capacity, mood, and quality of life in patients with PCC, and (II) to determine whether they are superior to conventional exercise.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable covid19
Started Jul 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 28, 2021
CompletedFirst Posted
Study publicly available on registry
July 30, 2021
CompletedStudy Start
First participant enrolled
July 30, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 27, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
February 27, 2022
CompletedSeptember 8, 2025
September 1, 2025
7 months
July 28, 2021
September 2, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
visual Analogue Scale
8th week
Secondary Outcomes (5)
hospital anxiety and depression scale-Depression
0th and 8th week
hospital anxiety and depression scale-Anxiety
0th and 8th week
Fatigue severity scale
0th and 8th week
Short Form-12
0th and 8th week
6 minutes walking test
0th and 8th week
Study Arms (2)
Virtual Realty
EXPERIMENTALVirtual reality exercises were implemented semi-immersively in the Kinect Sports Rivals program via the Microsoft Xbox One Kinect game console and Kinect V2 infrared camera. Participants were positioned 2 meters away from a 55-inch LCD screen in a well-lit room. Motion-controlled video games, including tennis, bowling, soccer, target shooting, climbing, and jet ski racing, were played against a virtual opponent, starting at a basic difficulty level and increasing in difficulty based on the participant's ability to defeat their opponent. Game transitions and difficulty adjustments were provided by the physical therapist. Participants performed plyometric movements such as jumping and shooting, as well as limb and spine movements, to direct the avatar and ensured the coordination of their movements.
Conventional
ACTIVE COMPARATORFlexibility exercises were performed during the warm-up and cool-down periods of aerobic exercise for 3-5 minutes, consisting of static and dynamic upper and lower extremity stretching exercises in standing and sitting positions. Neuromuscular exercises were performed on the Bosu ball and balance board with eyes open and closed, using one or both feet. Aerobic exercise using a bicycle ergometer was performed for 20-30 minutes, depending on patient tolerance, starting at 60% of the age-determined maximum heart rate and increasing by 5% every 2 weeks (75% in the last 2 weeks). Strengthening exercises were performed for 10-15 minutes using dumbbells or sandbags targeting the large muscles of the upper and lower extremities. Initially, one set of strengthening exercises was performed with 8 repetitions targeting 6 different muscles at 50% of 1 RM intensity. Depending on patient tolerance, the exercise intensity was increased weekly to 70%, the number of muscles worked to 10, the number o
Interventions
Eligibility Criteria
You may qualify if:
- diagnosed with COVID-19 by polymerase chain reaction from an oropharyngeal or nasopharyngeal swab sample more than 90 days ago, and who had PCC symptoms for at least eight weeks
You may not qualify if:
- have been hospitalized due to COVID-19,
- have developed pneumonia or organ failure findings.
- have had an acute myocardial infarction in the last 2 years,
- have cardiovascular system disease such as uncontrolled hypertension, arrhythmia, aneurysm, cardiac failure,
- have undergone fracture or orthopedic surgery in the last 2 years,
- have a known chronic respiratory system disease,
- have widespread pain such as fibromyalgia syndrome
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sivas Cumhuriyet University
Sivas, 58050, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Musa Polat
Cumhuriyet University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 28, 2021
First Posted
July 30, 2021
Study Start
July 30, 2021
Primary Completion
February 27, 2022
Study Completion
February 27, 2022
Last Updated
September 8, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share
The plan will be shared by the corresponding author at the submission stage if requested.