NCT05922865Completed
The Effect of Smart Sensor Combined With APP for Individualized Precise Exercise Training in Long Covid-19
Tri-service General Hospital, National Defence Medical Center, Taipei, Taiwan
Source: ClinicalTrials.gov · Last updated 27 Apr 2025
Brief summary (registry, in English)
The coronavirus (COVID -19) has rapidly turned into a global pandemic. For patients diagnosed with COVID-19, it caused severe damage in the upper respiratory system and systemic complications, including the cardiovascular, mental, nervous, and musculoskeletal system. Previous research has indicated that these subsequent sequelae can reduce quality of life. (A. W. Wong et al., 2020) Studies have indicated that exercise training is beneficial to improve blood pressure, reduce cardiovascular factors, reduce complications, and relieve depression (J. Galloza et al., 2017) However, the current international research on the benefits of exercise rehabilitation and the improvement of quality of life in patients who have been infected with COVID-19 is still lacking. Under the international epidemic, it is pointed out that the importance of telerehabilitation has also been advocated worldwide. Previous systematic review indicated that no matter it is nervous, muscular or cardiac system disease, the efficacy of telerehabilitation is superior to face-to-face rehabilitation. The purpose of this study is to compare the effect between the intervention of KNEESUP smart knee assistive device, and the health education in routine outpatient after diagnosis of Long Covid-19.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 120 (actual)
- First submitted
- 26 Jun 2023
- Start date
- 11 Jul 2023
- Primary completion date
- 27 Feb 2024
- Lead sponsor
- Shang-Lin Chiang
- Diseases
- Long COVID and ME/CFS
- NCT number
- NCT05922865
What you commit to
- Study type: Interventional
- Participants enrolled: 120
- From 11 Jul 2023 to the primary completion date, 27 Feb 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- had neuromuscular injury or surgery in the lower limbs in the past six months
- had participated in other clinical trials or received other alternative treatments
Other illness
- diagnosed with transient ischemic attack or stroke
- had heart rhythm regulator
- had aggravated symptoms due to infection again
Other
- hospitalized during training
Who the study is looking for
- symptoms last at least one month after recovery
- without physical impairment
- understood verbal or non-verbal communication
- normal cognitive function
- were willing to participate in the study and accept random allocation
Age in the registry: 20 years to 80 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Tri-Service General Hospital Coordinator of this site? Confirm its status | Taipei | Taiwan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.