Post-COVID-19 Syndrome

8

Review clinical trials related to Post-COVID-19 Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Physical Functions and Lifestyle Behaviours in Post-COVID-19 Syndrome Based on Circadian Rhythms

Post-COVID-19 syndrome is associated with persistent symptoms such as fatigue, reduced physical activity, and impaired respiratory function. Circadian rhythm differences (chronotype) may influence lifestyle behaviors including physical activity, nutrition, and sleep patterns. This observational cross-sectional study aims to compare respiratory muscle strength, physical activity levels, and nutritional habits among individuals with post-COVID-19 syndrome according to their chronotype (morning, intermediate, and evening types). Additionally, genetic analysis of the CLOCK gene polymorphism will be performed to support objective evaluation of circadian rhythm differences. The findings of this study may help to better understand the role of circadian rhythm in post-COVID-19 syndrome and contribute to the development of individualized rehabilitation and lifestyle interventions.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Hacettepe UniversityUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Diagnosed with Post-COVID-19 Syndrome [+7]

Recent myocardial infarction or pulmonary embolism [+4]

Status: Recruiting

Effectiveness of Functional Respiratory Muscle Training in Post-COVID-19 Syndrome

This study aims to investigate the effects of core stabilization exercises and functional inspiratory muscle training (IMT) on various physiological and psychological parameters in individuals with post-COVID-19 syndrome. Participants diagnosed with post-COVID-19 syndrome will be randomly assigned to two groups using stratified computer-assisted randomization. One group will undergo an 8-week core stabilization training, while the other will receive combined core stabilization and IMT training. Exercise training will be conducted three times a week, with each session lasting 50 minutes. Comprehensive pre- and post-intervention assessments will be conducted, including exercise capacity, respiratory and peripheral muscle strength, trunk endurance, balance, anxiety, depression, and fatigue levels. The primary outcome measures are respiratory muscle strength and trunk endurance. Participants must be aged 18-65 years, have at least a primary education level, speak Turkish, and be classified as level 2-3 on the Post-COVID-19 Functional Status Scale (PCFS). Eligible participants will be referred by the Internal Medicine Department at Hacettepe University. The study will utilize various assessment tools, including maximal inspiratory/expiratory pressure (MIP/MEP) tests, Functional Movement Screen (FMS), plank and Sorenson endurance tests, the Timed Up and Go Test for balance, handgrip and knee extension strength tests, body composition analysis, and the SF-36 quality of life questionnaire.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Hacettepe UniversityUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

Diagnosed with Post-COVID-19 Syndrome. [+6]

History of recent myocardial infarction or pulmonary embolism. [+3]

Status: Recruiting

Transcranial Pulse Stimulation (TPS) in Post-COVID-19

The objective of the present study is to demonstrate treatment efficacy of transcranial pulse stimulation for patients with Post-COVID-19 related neurological symptoms (fatigue, cognitive deficits, mood deterioration). Fatigue, as measured by the Fatigue Impact Scale (FIS), will represent the primary outcome variable. The verum treatment will be compared to a sham (placebo) condition.

Participants needed: 102
Trial details
Age: 20-80Biological sex: AllType: InterventionalSponsor: Medical University of ViennaUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

Signed written informed consent [+5]

Clinically relevant realization of pre-COVID diseases with similar symptoms as P... [+15]

Status: Recruiting

Effects of Kneipp Hydrotherapy in Post-COVID-19 Patients

This randomized controlled study evaluates the effects of cold water hydrotherapy in patients with Post-COVID Syndrome. The primary aim is to assess changes in quality of life compared to an usual care setting without hydrotherapy treatment.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Eggensberger OHGUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

Diagnosis of Post-COVID Syndrome (ICD-10 code: U08.9) [+3]

Existing contraindications for Kneipp hydrotherapy like severe cardiovascular di... [+1]

Status: Recruiting

Pursuing Reduction in Fatigue After COVID-19 Via Exercise and Rehabilitation (PREFACER): A Randomized Feasibility Trial

Long COVID is a complex condition that affects approximately 1.4 million Canadians following SARS-CoV-2 infection. Fatigue is the most common symptom of Long COVID. This feasibility trial will evaluate a new rehabilitation program called COVIDEx for treating fatigue after COVID-19, and compare its effectiveness to the standard treatment currently used. The experimental treatment group will receive an 8-week multi-modal rehabilitation program with two 50-minute sessions per week. 60 participants will be recruited, randomly assigned to the COVIDEx program or standard of care (SoC) and followed for 24 weeks.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Lawson Research Institute of St. Joseph'sUpdated: Aug 1, 2025Locations: 1
Eligibility criteria

Adults of at least 18 years of age [+9]

Active SARS-CoV-2 infection [+6]

Status: Recruiting

Yoga Versus Health Education for the Treatment of Persistent Fatigue in Patients With Post COVID-19 Syndrome

Evaluation of the short- and medium-term effect of a yoga intervention in addition to routine care compared to health education in addition to routine care on fatigue in patients with post covid syndrome.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University Hospital TuebingenUpdated: Jul 10, 2025Locations: 1
Eligibility criteria

Confirmed COVID-19 diagnosis [+4]

Chronic medical conditions or regular use of medications associated with fatigue [+6]

Status: Recruiting

Retinal Neurovascular Coupling in Patients Previously Infected With COVID-19

The Study objective is to measure retinal neurovascular coupling and blood flow parameters in patients previously infected with COVID-19, long COVID-19 and healthy age- and sex- matched control subjects

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Medical University of ViennaUpdated: May 16, 2025Locations: 1
Eligibility criteria

Men and women aged over 18 years [+17]

Symptoms of a clinically relevant illness in the 3 weeks before the first study... [+23]

Status: Recruiting

Cohort Follow-up of Epidemic and Neuroimaging for Patients During the 1st Wave of the COVID-19 in China

Our main objective is to analyze the development of physical impact, mental health and blood profile over follow-up time during the 1st wave of the COVID-19. Besides, we aim to establish a database of post-COVID-19 based on simultaneous cortico-spinal magnetic resonance imaging data to identify high-risk patients with long COVID and prevent the neurological symptoms evolution, optimize the tactics of management in China.

Participants needed: 600
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: First Affiliated Hospital Xi'an Jiaotong UniversityUpdated: Feb 27, 2023Locations: 1
Eligibility criteria

Not listed