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Not yet recruitingNCT06832527Updated Feb 20, 2025

Use of Virtual Reality to Improve Sensorimotor Function in Patients with Traumatic Wrist and Hand Injuries

An interventional study of Rehabilitation treatment and Virtual Reality games in Wrist Injury, sponsored by University of Malaga. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-02-20.

Sponsored by University of Malaga · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 6 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
79
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this randomized clinical trial is to compare how the incorporation of Virtual Reality could influence in proprioception, kinesiophobia, functionality and catastrophism in people that are undergoing a rehabilitation treatment after a wrist fracture. The principal questions it aims to answer are:

  • Evaluate the effect of using virtual reality added to standard rehabilitation of wrist injuries in proprioception impairment.
  • Evaluate the effect of using virtual reality on psychological factors as kinesiophobia and catastrofism.
  • Evaluate the effect of using virtual reality in functionality on wrist-injured patients.

Intervention will be:

  • Control group: participants of this group will receive conventional rehabilitation of the wrist, plus a specific proprioceptive exercise program.
  • Experimental group: participants of this group will receive the same treatment as the control group but adding virtual reality games at the end of the session.

Researchers will compare control and experimental group to see if an implantation of Virtual Reality could had benefits on function, kinesiophobia, catastrofism and proprioception.

02

Conditions studied

  • Wrist Injury

Keywords

  • wrist injury
  • proprioception
  • virtual reality
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In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's planned enrollment of 79 is above the median of 52 across 3,239 interventional studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

University of Malaga is the lead sponsor of 118 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult (equal or more than 18 y/o).
  • Suffering wrist injury
  • Agree and sign informed consent.

Exclusion criteria

Exclusion Criteria:

  • Not had suffered a wrist injury
  • Suffer from any mental, cognitive, neurological or musculoskeletal disorder
  • Have cervical pathology/impairment
  • Have visual or balance problems
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
79 participants (estimated)

Study arms

  • Active comparator
    Conventional rehabilitation

    Conventional rehabilitation treatment for the wrist plus a specific proprioceptive exercise program.

    Other: Rehabilitation treatment

  • Experimental
    Rehabilitation+virtual reality

    Conventional rehabilitation treatment for the wrist plus a specific proprioceptive exercise program and virtual reality games

    Other: Rehabilitation treatment · Other: Virtual Reality games

Interventions

  • OtherRehabilitation treatment

    ROM, strength, stretch and proprioception exercises

  • OtherVirtual Reality games

    Virtual Reality games using META QUEST PRO glasses

06

What researchers measure

Primary outcomes

  1. Proprioception

    Assessment of proprioception impairment using Joint Position Sense Test (JPST). Punctuation will be the difference between the asked position and the patient's replication. The test will be repeated with open and closed eyes.

    Time frame: Baseline, 1 and 3 months

Secondary outcomes

  1. Kinesiophobia

    Fear of movement, assessed with Tampa Scale for Kinesiophobia (TSK) which has 17 items with Likert's answers. Punctuation goes from 17 to 68 points, where \<37 points means a low level of kinesiophobia and \>37 a high level.

    Time frame: Baseline, 1 and 3 months

  2. Catastrophism

    Catastrophizing pain assessed with Pain Catasthrophizing Scale (PCS) which has 13 items with Likert's answers. Punctuation goes from 0 to 52 points, where 0-20 points means a low catastrophism, 21-30 points moderate catastrophism and \>30 points a high catastrophism.

    Time frame: Baseline, 1 and 3 months

  3. Function

    Functionality of the upper limb assessed with QuickDASH which has 11 items. Punctuation goes from 0 to 100, where 0 means no disability and 100 maximum disability.

    Time frame: Baseline, 1 and 3 months

  4. Hand and Wrist function

    Assessed with Patient-Rated Wrist Evaluation (PRWE) which has 15 items punctuated from 0 to 10. Punctuation goes from 0-100 where 0 means no disability and 100 maximum disability.

    Time frame: Baseline, 1 and 3 months

  5. Range of motion

    Range of motion of the wrist and fingers using a goniometer.

    Time frame: Baseline, 1 and 3 months

  6. Force Sense

    GRIP's force sense assessed with Force Sense Test (FST), where punctuation is the difference between the asked and replicated force.

    Time frame: Baseline, 1 and 3 months

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06832527
Lead sponsor
University of Malaga
Responsible party
Leire Cruz-Gambero (Occupational therapist, University of Malaga) — Principal investigator
First posted
Feb 18, 2025
Start date
Feb 25, 2025 (estimated)
Primary completion
Apr 2025 (estimated)
Completion
Jul 2025 (estimated)
Last update
Feb 20, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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