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NCT Number: NCT06739837

Comparison of the Effect of a Non-immersive VRE and CT in Patients With Tennis Elbow

This study investigates the comparative effectiveness of non-immersive virtual reality (VR) therapy and conventional physiotherapy in managing tennis elbow (lateral epicondylitis). Tennis elbow is a painful condition often characterized by chronic pain, reduced grip strength, and limited functionality.

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This study is active but is not currently recruiting participants.

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Key information

Conditions

Tennis Elbow Arm Injuries Elbow Injuries Elbow Tendinopathy Muscular Diseases Musculoskeletal Diseases Tendinopathy Tendon Injuries Wounds and Injuries

Age range

20 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Samahni, Near thq hospital samahni azad kashmir

Kashmir, Azad Kashmir, Pakistan

About this study

Conventional treatment approaches, including manual therapy and strengthening exercises, have been widely used but may not fully address the long-term rehabilitation needs of every patient. Virtual reality, an emerging tool in rehabilitation, has the potential to enhance patient engagement and adherence by providing an interactive therapeutic environment. Participants will be divided into two groups: one receiving VR therapy and the other conventional therapy, with each intervention lasting six weeks. Outcome measures include pain intensity (VAS), functional disability (DASH), patient satisfaction (PRTEE), grip strength, range of motion (ROM), and adherence rates. This study aims to determine if VR therapy can offer superior benefits over conventional

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 25 to 50 years.
  • Patient diagnosis with lateral epicondylitis.
  • Patients that a medical doctor will be formally diagnosed to have tennis elbow, that is, lateral epicondylitis.
  • Patients who have specific pain and function impairment associated with tennis elbow.
  • Patients giving written consent to participate in the study. Willing to participate and provide informed consent.

Exclusion criteria

  • Patients with neurological conditions whereby they have abnormal functioning of their arms.
  • Any previous surgical intervention for tennis elbow The presence of other significant musculoskeletal diseases in the upper extremity Severe cardiovascular or neurological disorders.

Treatment and study plan

traditional physiotherapy

Diagnostic Test

Participants in this arm will undergo traditional physiotherapy exercises for managing tennis elbow.

Non-immersive VR therapy

Combination Product

Participants undergo a VR-based rehabilitation program targeting tennis elbow symptoms. Sessions last 30 minutes, conducted 3 times per week for 6 weeks. Exercises focus on improving grip strength, wrist flexibility, and functional movement through interactive VR environments that visually engage the affected arm, promoting adherence and motivation without full immersion. The VR setup includes headsets or screens that enable visual interaction, enhancing the rehabilitation experience. The goal is to alleviate pain, increase range of motion, and restore muscle strength.

Primary outcomes

  1. Visual Analog Scale (VAS)

    Time frame: 12 Months

    The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain.

  2. Handheld Dynamometer

    Time frame: 12 Months

    This instrument is scored using force production in kilograms (0-90) or pounds (0-200). Standardized procedure for positioning of instrumen

Sponsors and collaborators

Lead sponsor

Superior University

Other

Registry information

Official study title

Comparison of the Effect of a Non-immersive Virtual Reality Environment and Conventional Treatment in Patients With Tennis Elbow

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Dec 18, 2024
Registry last updated
Dec 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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