Effects of Physiotherapy Via Telerehabilitation in Patients With COVID-19

NCT ID: NCT06251011

Last Updated: 2024-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-09

Study Completion Date

2024-06-04

Brief Summary

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This study aims to evaluate the effects of Physiotherapy Via Video Calls on Cardiopulmonary Functions, Physical Function, Cognitive Function, Activity Daily Livings, and Quality of Life in Patients With COVID-19.

Detailed Description

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A 2-armed, parallel-group, randomized controlled trial was conducted at Chulabhorn Hospital, Thailand on a convenience sample of patients who tested positive for COVID-19 using RT-PCR.

Conditions

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COVID-19 Long COVID-19 Cardiopulmonary Function Physical Function

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Control group

Receive an advice and a leaflet for cardiopulmonary rehabilitation.

Group Type NO_INTERVENTION

No interventions assigned to this group

Physiotherapy group

Receive the physical therapy training via video call (Pulmonary training, Calisthenic exercise, Upper and lower limbs strengthening exercise, Core stabilizer exercise, Aerobic exercise) at day 3, 6, 9, 12, 16, and 21 after positive in COVID-19 testing and also receive advise and a leaflet for cardiopulmonary rehabilitation.

Group Type EXPERIMENTAL

Exercise training

Intervention Type BEHAVIORAL

1. Physical therapy training via video call
2. An advise and a leaflet for cardiopulmonary rehabilitation

Interventions

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Exercise training

1. Physical therapy training via video call
2. An advise and a leaflet for cardiopulmonary rehabilitation

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age between 20-60 years old
* Positive in COVID-19 testing
* Good communication and understanding
* Independent mobility

Exclusion Criteria

* Cannot complete the study protocol
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chulabhorn Hospital

OTHER

Sponsor Role lead

Responsible Party

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Pooriput Waongenngarm, PT, PhD

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Pooriput Waongenngarm, PhD

Role: PRINCIPAL_INVESTIGATOR

Chulabhorn Royal Academy

Locations

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Chulabhorn hospital

Lak Si, Bangkok, Thailand

Site Status

Countries

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Thailand

Other Identifiers

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EC014/2565

Identifier Type: -

Identifier Source: org_study_id

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