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NCT05118659 Clinical Trial

Mulligan Therapy Effects In Healthy Subjects With Induced Vertigo

Vertigo Clinical Trial

Official title:
Mulligan Therapy Effects In Healthy Subjects With Induced Vertigo. A Randomized And Controlled Clinic Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05118659
Other study ID # CSEULS-PI-198/2018
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 3, 2018
Est. completion date June 28, 2018

Study information
Verified date November 2021
Source Centro Universitario La Salle
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This analysis aims to evaluate the immediate effect that cervical sustained natural apophyseal glides (SNAGs) have on a group of individuals with induced vertigo by a caloric vestibular stimulation.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date June 28, 2018
Est. primary completion date June 4, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 44 Years
Eligibility Inclusion Criteria: - Healthy subjects, - Age 18-44 years. Exclusion Criteria: - Consume of antipsychotics, antidepressants, antiarrythmics and/or anticonvulsivants - Hippoacusia - Auditory diseases - Peripheral or central vestibulopathies - Cerviogenic dizziness - Balance disorders - Nistagmus - Oculomotor nerve dysfunctions - Migraine - Cervical osteoporosis, lashing or fracture - Discal cervical hernia - Cervical neuropathy - Psychriatic disorders - Epilepsy - Pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• sustained natural apophyseal glides
It consists on a sustained apophyseal glides in a postero-anterior direction on C2 with a dose of three series of ten repetitions each
• SHAM SNAG
Subjects on SNAG group received a simulation of the contact used for the SNAGs, without any vertebral glide, and with an active cervical extension

Locations
Country Name City State
Spain CSEU La Salle Madrid
Spain Jose V Leon Hernandez Madrid

Sponsors (1)
Lead Sponsor Collaborator
Centro Universitario La Salle

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary vHIT (Video Head Impulse Test) Detection of peripheral vestibular deficits and their recovery 15 minutes
Secondary Anxiety state-trait anxiety was measured at the beginning of the study using the Spanish version of the trait-state anxiety inventory (STAI) 5 minutes
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