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3R Rehabilitation Management of COVID-19 Survivors

T

The Hong Kong Polytechnic University

Status

Unknown

Conditions

Covid19

Treatments

Other: Cardiopulmonary exercise (centre-based)
Other: Cardiopulmonary exercise (online-based)

Study type

Interventional

Funder types

Other

Identifiers

NCT04892979
HSEARS20200912001

Details and patient eligibility

About

It is to explore the temporal relationships between physical fitness, cognitive, psychosocial functions, and health-related quality of life (HRQoL) in COVID-19 survivors over the first 15 months; and to determine the effects of centre-based (CBR), online-based cardiopulmonary rehabilitation (OBR), and combined centre- and online-based rehabilitation (COBR) on survivors with initially suboptimal pulmonary functions.

Enrollment

400 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • COVID survivor at hospital discharge or 6-month post-disease onset
  • Medically stable with an Abbreviated Mental Test (AMT) scores of > 6 out of 10

Exclusion criteria

  • Having contraindications to exercise
  • Physical Activity Readiness Questionnaire (PAR-Q) reveals unsafety
  • Cannot understand Cantonese

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

400 participants in 3 patient groups

Centre-based
Experimental group
Description:
Centre-based exercise cardiopulmonary rehabilitation program for 6 weeks
Treatment:
Other: Cardiopulmonary exercise (centre-based)
Online-based
Experimental group
Description:
Online-based exercise cardiopulmonary rehabilitation program for 6 weeks
Treatment:
Other: Cardiopulmonary exercise (online-based)
Combined
Experimental group
Description:
Combined centre- and online-based exercise cardiopulmonary rehabilitation program for 6 weeks
Treatment:
Other: Cardiopulmonary exercise (online-based)
Other: Cardiopulmonary exercise (centre-based)

Trial contacts and locations

4

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Central trial contact

Siu Ngor Fu, PhD

Data sourced from clinicaltrials.gov

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