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Tele-Rehabilitative Exercise Training Program in Nurses With Long COVID

Status

Completed

Conditions

Quality of Life (QOL)
Long COVID
Fatigue
Nurses
Cardiorespiratory Fitness
Tele-rehabilitation
Exercise
Stress

Treatments

Behavioral: Healthy consulation
Device: wearable device

Study type

Interventional

Funder types

Other

Identifiers

NCT06840873
c202305117

Details and patient eligibility

About

Long COVID can cause a decline in cardiorespiratory fitness, resulting in fatigue and negative impacts on individuals' quality of life (QoL), particularly in nurses who play a crucial role in public health. Combining with reduced cardiorespiratory fitness and suffering from a spectrum of long-COVID symptoms might substantially exaggertate fatigue, perceived stress, and reduce willingness to work for hospital nurses. Therefore, this study aimed to evaluate the effectiveness of tele-rehabilitative exercise on fatigue, perceived stress, symptom severity of long COVID, and QoL in this population.

Full description

The intervention is an extra 8-week tele-rehabilitative exercise program (3 aerobic and 2 strengthing exercise sessions/week at a moderate intensity, 30 min/session), monitored through a wearable devices and a mobile App. The evaluation of the rehabilitation results can be presented as a data chart, and the treatment effects are also clearly presented. Outcome measures were assessed at baseline, 4, and 8 weeks. Cardiorespiratory fitness was measured before and after the intervention via cardiopulmonary exercise tests.

Enrollment

68 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • nurses older than 20 years of age
  • have reported a positive result on a COVID-19 rapid test or nucleic acid test
  • one or more of the following symptoms for more than four weeks: fatigue, discomfort after physical or mental exertion, fever, cardiopulmonary symptoms such as difficulty breathing or shortness of breath, cough, chest pain, or palpitations (CDC, 2022)
  • able to perform activities independently without assistance
  • total score of 36 or higher on the Fatigue Severity Scale (FSS), confirming fatigue symptoms, and report that these symptoms either appeared after the infection or worsened following the infection

Exclusion criteria

  • without the equipment to install a mobile application (APP)
  • unsuitable for wearing devices due to any leg diseases
  • unable to engage in aerobic or strength training due to neurological or musculoskeletal disorders
  • pregnancy
  • cancer
  • absolute and relative contraindications for cardiopulmonary testing or exercise training
  • unsuitable for participation in this study by a rehabilitation specialist;
  • regular exercisers

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

68 participants in 2 patient groups, including a placebo group

Health consultation
Placebo Comparator group
Description:
The participants with healthy consultation do aerobic training at home
Treatment:
Behavioral: Healthy consulation
wearable device
Experimental group
Description:
The participants with wearable device do exercise training at home
Treatment:
Device: wearable device

Trial contacts and locations

1

There are currently no registered sites for this trial.

Timeline

Last updated: Apr 04, 2025

Start date

Nov 02, 2023 • 1 year and 6 months ago

End date

Jun 30, 2024 • 10 months ago

Today

May 08, 2025

Sponsor of this trial

Lead Sponsor

Data sourced from clinicaltrials.gov