Clinical trial Recruiting at 1 site Interventional Ages 18 to 70

Vestibular rehabilitation for adults having surgery for a unilateral vestibular schwannoma

Official title: Prospective Comparative Clinical Study of Three Parallel Cohorts on the Efficacy of Pre- and Post-surgical Vestibular Rehabilitation With or Without Rotary Stimulation in Patients With Vestibular Schwannoma

Run by Universitat Autonoma de Barcelona · NCT07364955 · Data updated 2026-11-12

This trial tests whether home-based vestibular telerehabilitation before and after surgery, and adding preoperative rotatory chair sessions, can help adults recover balance and reduce dizziness after removal of a unilateral vestibular schwannoma.

More Vestibular Schwannoma trials

Quick facts

Study typeInterventional
Ages18 Years to 70 Years
SexAll
Enrollment75 (estimated)
SponsorUniversitat Autonoma de Barcelona
Academic / other
Locations1 site (Badalona, Barcelona)
StatusRecruiting
StartedSeptember 1, 2025
Main results expectedMarch 31, 2027
Study endsDecember 31, 2027
Registry record updatedJanuary 23, 2026
Trial IDNCT07364955 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–70 with a unilateral vestibular schwannoma measuring 1.5–4 cm who do not have major neurological, cerebrovascular, or musculoskeletal exclusions.

Probably not a fit

Patients with bilateral vestibular disease, degenerative neurological conditions, prior cerebrovascular disease, significant musculoskeletal deformities, or tumors outside the 1.5–4 cm size window are unlikely to receive benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, non-randomized, three-arm study compares no-intervention standard care, a structured home-based telerehabilitation program (ReHub) performed 3 weeks before and 3 weeks after surgery, and the same telerehab plus six supervised preoperative rotatory chair sessions. Participants undergo vestibular function testing (vHIT), dizziness questionnaire (DHI), posturography, and monitoring of hospital length of stay to quantify postoperative vestibular compensation. The rotatory chair protocol uses a progressive increase in rotational velocity and post-rotation visual fixation tasks to prime vestibular adaptation before surgery. Outcomes will compare balance, dizziness, gaze stabilization, and recovery time across the three cohorts.

Why it matters

Potential benefit: If successful, patients could regain balance and reduce dizziness more quickly after surgery, possibly shortening hospital stays and speeding return to daily activities.

How similar studies have gone: Vestibular rehabilitation is an established approach that improves compensation after vestibular loss, but preoperative rotatory chair priming is a novel strategy with limited prior data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age between 18 and 70 years
* Tumor size between 1.5 cm and 4 cm
* Unilateral vestibular schwannoma

Exclusion Criteria:

* Degenerative neurological conditions
* History of cerebrovascular disease
* Musculoskeletal deformities

Where it's running

  • Hospital Universitari Germans Trias i Pujol
    Badalona, Barcelona, Spain
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.