Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07364955

Vestibular Rehabilitation Protocol in Unilateral Vestibular Schwannoma

Led by Albert Torrents Torrero · Updated on 2026-01-23

75

Participants Needed

1

Research Sites

121 weeks

Total Duration

On this page

Sponsors

A

Albert Torrents Torrero

Lead Sponsor

G

Germans Trias i Pujol Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Brief Summary The purpose of this clinical trial is to evaluate whether different strategies of vestibular rehabilitation, performed before and after surgery, can improve recovery in adults diagnosed with unilateral vestibular schwannoma. The main questions the study aims to answer are: Does preoperative vestibular telerehabilitation improve postoperative vestibular compensation compared with no intervention? Does adding preoperative rotatory chair stimulation to telerehabilitation lead to greater improvements in balance, dizziness, or hospital length of stay? The study includes three comparison groups: No-intervention group: Participants do not receive pre- or postoperative rehabilitation, but complete all study assessments (vHIT, DHI, posturography, and hospital length of stay). Telerehabilitation group: Participants complete a structured home-based vestibular telerehabilitation program (ReHub) for 3 weeks before surgery and again for 3 weeks after surgery. Rotatory Chair + Telerehabilitation group: Participants receive the same telerehabilitation program as the telerehabilitation group, plus six supervised sessions of preoperative rotatory chair stimulation (two sessions per week for three weeks), following a progressive protocol in the ENT department using a CE-marked clinical rotatory chair. Participants will: Attend routine preoperative and postoperative assessments (vHIT, posturography, and DHI). Complete home-based vestibular exercises through a digital telerehabilitation platform (Groups 2 and 3). If assigned to the Rotatory Chair + Telerehabilitation group, attend six in-hospital sessions of controlled rotatory chair stimulation during the three weeks before surgery. Undergo follow-up evaluations at 4 and 12 weeks after surgery. This study aims to determine whether structured vestibular training conducted before and after surgery can enhance postoperative compensation and reduce symptom burden in patients undergoing vestibular schwannoma surgery.

CONDITIONS

Official Title

Vestibular Rehabilitation Protocol in Unilateral Vestibular Schwannoma

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 70 years
  • Tumor size between 1.5 cm and 4 cm
  • Diagnosis of unilateral vestibular schwannoma
Not Eligible

You will not qualify if you...

  • Presence of degenerative neurological conditions
  • History of cerebrovascular disease
  • Presence of musculoskeletal deformities

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Hospital Universitari Germans Trias i Pujol

Badalona, Barcelona, Spain, 08916

Actively Recruiting

Loading map...

Research Team

A

Albert Torrents Torrero, PT, MsC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here