The effect of proprioceptive training on tinnitus, muscle strength and functional capacity in individuals who have sequelae after having had COVID-19: Randomized Clinical Trial

Not Applicable

Recruiting

• Conditions: C01.748.214; Coronavirus, as a cause of diseases classified in other chapters

• Registration Number: RBR-7yh559g
• Lead Sponsor: niversidade Federal de Pernambuco

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-07-21
• Study Completion: 2022-10-10
• Results First Posted: 2022-11-10
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Individuals who have been affected by Covid-19 proven by laboratory examination; Be functionally independent; Absence of severe neurological disease, vascular disorder, labyrinthitis and blindness; Patient without severe foot deformity, requiring therapeutic footwear, and in the spine and who do not have orthopedic deficiencies; Do not use mobility aids; No history of fractures in the lower limbs and spine in recent years.

Exclusion Criteria

Individuals with COVID-19; have uncontrolled hypertension, that is, systolic blood pressure at rest (?180 mmHg) and/or diastolic blood pressure at rest (?110 mmHg); uncontrolled arrhythmia; active myocarditis; signs respiratory distress at rest; oxygen saturation less than 88%; acute systemic illness or fever; resting heart rate less than 50 and greater than 100 beats per minute; nausea; dizziness; shortness of breath and/or severe fatigue; drop in 4% of oxygen saturation in relation to the resting value and values ??less than 88%; excessive sweating; anxiety crisis; palpitations; pain or tightness in the chest; presents pain during training; Inadequate execution of activities during the intervention procedure; making it impossible to obtain data; Not signing the consent form

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement of tinnitus, evaluated by the THI-Tinnitus Handicap Inventory test (this used to evaluate the severity of tinnitus), of dizziness, evaluated by the Berg balance test and by the MiniBesttest, of muscle strength, evaluated by the dynamometer, as well as of functional capacity , evaluated by the 6-minute walk test and the Time-Up-To-Go (TUG). Data collected during the 12 weeks of intervention.<br>No Secondary Outcome Expected.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected