Virtual reality offers new hope for seniors living in fear of movement
NCT ID NCT07607899
First seen Jun 27, 2026 · Last updated Sep 11, 2026 · Updated 2 times
Summary
This study tests a program that combines a pain education class with immersive virtual reality sessions to help older adults with chronic pain overcome their fear of movement. Participants will be randomly assigned to receive either the education alone or the education plus up to eight VR sessions over a month. The goal is to see if this approach is practical and can reduce fear, improve confidence, and encourage safe physical activity.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 65 years or older * Able to understand and communicate in French * Chronic pain lasting 6 months or longer * Average pain intensity of 3 or greater on a 0-10 Numeric Rating Scale during the week prior to enrollment * Score greater than 25 on the 11-item Tampa Scale of Kinesiophobia (TSK-11) * No neurocognitive impairment (Mini-Mental State Examination \[MMSE\] ≥ 24), or mild neurocognitive impairment (MMSE 18-24) with preserved capacity to consent (University of California Brief Assessment of Capacity to Consent \[UBACC\] score ≥ 12) * Normal or corrected-to-normal visual acuity Exclusion Criteria: * Severe motion sickness or intolerance that would prevent safe use of a virtual reality headset (experimental group only) * Medical condition that would prevent safe participation in rehabilitation activities * Presence of open wounds or infection at painful or contralateral sites
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CISSS de Chaudière-Appalaches
RECRUITINGSainte-Marie, Quebec, Canada
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CIUSSS de la Capitale-Nationale
RECRUITINGQuébec, Quebec, Canada
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Other studies related to the condition(s) this trial covers.
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