Study on Post-Acute COVID-19 Syndrome in Improvement of COVID-19 Rehabilitated Patients by Respiratory Training

NCT06165835 | Completed

• 1 other identifier: A202305044
• Study Type: interventional
• Target: 90
• Locations: 1 country
• Sites: 1

Brief Summary

Since the emergence of Corona Virus Disease 2019(COVID-19), it has spread rapidly around the world, And it has had a profound impact on the lives and health of people around the world, most of the COVID-19 positive patients are 3-4 weeks after the onset of infection patients can turn negative and recover, however, increasing observational data suggest that these patients long-term or recurring symptoms such as: fatigue, palpitations, cognitive impairment, dyspnea, anxiety, chest tightness and Pain, etc., symptoms may last at least two months or even longer (for example, up to 12 months), the patient's quality of life and The ability to work and social activities also decline accordingly. Therefore, in addition to the acute symptoms after infection, patients also face the same. The challenge of long-term health sequelae associated with COVID-19.

Conditions

COVID-19; Post-Acute COVID-19 Syndrome; Dyspnea; Incentive Spirometer

Outcome Measures

Primary Outcomes (1)

• Oxygen requirements, blood draw values

  Oxygen requirements, blood draw values

  6 WEEKS

Study Arms (5)

Experimental

NO INTERVENTION

Patients who have recovered from COVID-19

Three months after recovering from COVID-19

EXPERIMENTAL

Patients who have from COVID-19 in three months

Device: breathing training

Six months after recovering from COVID-19

EXPERIMENTAL

Patients who have from COVID-19 in three to six months

Device: breathing training

Nine months after recovering from COVID-19

EXPERIMENTAL

Patients who have from COVID-19 in six to nine months

Device: breathing training

Twelve months after recovering from COVID-19

EXPERIMENTAL

Patients who have from COVID-19 in nine to twelve months

Device: breathing training

Interventions

breathing training DEVICE

Breathing training for six weeks.

Also known as: Incentive Spirometer

Nine months after recovering from COVID-19; Six months after recovering from COVID-19; Three months after recovering from COVID-19; Twelve months after recovering from COVID-19

Eligibility Criteria

• Age: 20 Years - 90 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• \. Patients who have recovered from COVID-19

You may not qualify if:

• Have suffered from within one year. Those who have recovered from COVID-19 must present proof of diagnosis, such as a medical certificate or screening results, etc., and ICD10 when seeking medical treatment The diagnostic codes are: U07.1 Confirmed COVID-19 virus infection, U09.0 Severe specific infectious pneumonia (COVID-19), unspecified.
• adult, aged 20-90
• conscious mind and behavior normal mental state examination (Mini-Mental State Examination, MMSE) score \> 21 points.
• Those who can communicate in verbal or non-verbal ways and understand Chinese and Taiwanese.
• are willing to participate in the research and agree to accept random machine dispatcher

Sponsors & Collaborators

• Tri-Service General Hospital: lead

Study Sites (1)

Tri Service General Hospital Sonshan Branch

Taipei, 105309, Taiwan

Location

MeSH Terms

Conditions

COVID-19; Post-Acute COVID-19 Syndrome; Dyspnea

Interventions

Breathing Exercises

Condition Hierarchy (Ancestors)

Pneumonia, Viral; Pneumonia; Respiratory Tract Infections; Infections; Virus Diseases; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Lung Diseases; Respiratory Tract Diseases; Post-Infectious Disorders; Chronic Disease; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Respiration Disorders; Signs and Symptoms, Respiratory; Signs and Symptoms

Intervention Hierarchy (Ancestors)

Mind-Body Therapies; Complementary Therapies; Therapeutics; Exercise Movement Techniques; Physical Therapy Modalities

Study Officials

• Yao-Hsiang Chen

  Tri Service General Hospital Sonshan Branch

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: assistant hand nurse

Study Record Dates

• First Submitted: December 9, 2023
• First Posted: December 12, 2023
• Study Start: July 1, 2023
• Primary Completion: December 30, 2024
• Study Completion: December 30, 2024
• Last Updated: April 3, 2025

Record last verified: 2025-03

Locations

TW (1)