Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Musculoskeletal Pain
  • Rehabilitation
  • Vestibular Disease
Type
Interventional
Phase
Not Applicable
Design
Allocation: Non-RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: After 1 year participants who still have dizziness complaints will be offered one of two interventions: Group-based vestibular rehabilitation combining cognitive intervention, vestiular exercises and body awareness therapy Exergaming intervention with virtual reality exercises using data games and videos, and other balance exercises. Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 67 years
Gender
Both males and females

Description

Patients referred to an tertiary otorhinolarynglogical clinic due to dizziness will be invited to participate in the study. The aims are to examine the prevalence, extent and distribution of musculoskeletal pain in patients with prolonged dizziness, and to investigate the associations between muscul...

Patients referred to an tertiary otorhinolarynglogical clinic due to dizziness will be invited to participate in the study. The aims are to examine the prevalence, extent and distribution of musculoskeletal pain in patients with prolonged dizziness, and to investigate the associations between musculoskeletal pain, dizziness symptoms, psychological and physical function and health-related quality of life. Furthermore, the aim is to monitor the natural course of the dizziness symptoms and functional status in these patients, and examine risk factors for prolonged disability after 6 and 12 months. The hypothesis is that muscle pain and distress at baseline may be independently associated with prolonged complaints at follow-up. Finally, patients who still are dizzy and have pain after 12 months will be invited to participate in one of two group interventions a) modified vestibular rehabilitation and b) virtual reality / exergaming. The interventions will be feasibility studies with a pre-post design.

Tracking Information

NCT #
NCT04241822
Collaborators
Haukeland University Hospital
Investigators
Study Director: Gro Anita F Flaten, ph.d. Western Norway University of Applied Sciences Study Director: Evelyn Neppelberg, ph.d. Haukeland University Hospital