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Study identifier: NCT06948500 Synced from ClinicalTrials.gov · July 29, 2026
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Effectiveness of an IVR-based Therapeutic Exercise Program With Altered Visual Feedback in Fibromyalgia Patients

Condition: Fibromyalgia  ·  Sponsor: Cardenal Herrera University

PhaseNA
Planned participants80
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The primary aim of this randomized controlled trial is to determine the efficacy of a 6-week immersive virtual reality (IVR)-based therapeutic exercise intervention, which manipulates visual proprioceptive input during exercise, for patients diagnosed with fibromyalgia (FM). Participants will be randomly allocated into two groups: an experimental group performing therapeutic exercises integrated with IVR featuring modified visual feedback, and a control group executing identical exercises without IVR integration. The primary outcome will assess the impact of fibromyalgia on daily activities, while secondary outcomes will comprehensively evaluate fatigue, sleep quality, severity of fibromyalgia symptoms, health-related quality of life, anxiety and depressive symptoms, fear-avoidance beliefs, pain catastrophizing, kinesiophobia, indicators of central sensitization, lumbar spine flexion and extension range of motion, somatosensory function, body perception distortion, muscle strength of the handgrip and quadriceps, functional mobility, lower limb strength, behavioral regulation concerning exercise adherence, and patient-reported experiences regarding IVR use. This trial seeks to elucidate whether incorporating IVR into therapeutic exercise protocols reduces the impact of fibromyalgia on patients' daily lives and improves physiological, psychological, and physical outcomes compared to traditional exercise approaches without IVR.

This description comes directly from the study's public registry record.

Talk to the study team

JUAN FRANCISCO LISÓN PÁRRAGA, PhD  ·  606503108  ·  JUANFRAN@UCHCEU.ES

Juan J Amer, PhD  ·  96136900  ·  juanjoamer@uchceu.es

Always discuss trial participation with your own doctor first.

Locations (1)

Juan Fco. LisónValencia, Valencia-valència, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06948500