Autonomic Telerehabilitation in patients with Vasovagal Syncope

Not Applicable

Recruiting

• Conditions: Vasovagal Syncope; C10.177

• Registration Number: RBR-64ktszb
• Lead Sponsor: niversidade Federal de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-07-18
• Last Update Posted: 22 August 2023
• Study Completion: 2024-05-01

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients with a clinical diagnosis of vasovagal syncope with at least 1 syncope episode or 2 pre-syncope episodes in the last 3 months; both sexes; aged between 18 and 65 years

Exclusion Criteria

Shift workers; patients with neurological diseases; diabetes mellitus; morbid obesity; pregnant women; previous cardiovascular events; obstructive sleep apnea; disabling illnesses; cognitive impairment; eye diseases that affect the pupillary reflex; history of anterior segment trauma; history of eye surgery; users of eye drops or systemic drugs that affect pupillary diameter; volunteers without internet access; patients who did not reach the minimum recommended performance in functional capacity tests

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected to find a decrease in the recurrence of vasovagal syncope or pre-syncope and an improvement in the quality of life in patients who participated in the telerehabilitation group when compared to patients belonging to the control group. The method used to verify the number of episodes of vasovagal syncope or pre-syncope is monitoring through the syncope diary in both groups. To assess patients' quality of life, the World Health Organization Quality of Life-bref questionnaire is used

Secondary Outcome Measures

Name	Time	Method
o secondary completions expected