Clinical Trials in Japan / NCT05193136
Recruiting
Observational
Sleep Hygiene, Sarcopenia, and Cognitive Function in Respiratory Disease
NCT05193136 · tracked via the Priya Life Science Japan tracker
Condition(s) studied
Sleep HygieneSarcopeniaCognitive FunctionCOPDIPF
Study summary
We aim to clarify the relationship between sleep hygiene and the onset of sarcopenia or cognitive dysfunction using sleep time, arousal, and sleep quality as indicators in COPD or IPF patients, and clarify the effects of sleep hygiene on disease progression and life prognosis.
Eligibility
Inclusion Criteria:
* Subjects with COPD or IPF.
Exclusion Criteria:
* Subjects who have been hospitalized for exacerbation of respiratory failure within 1 month of study participation
* Subjects who have already been diagnosed with sarcopenia or cognitive dysfunction
* Subjects receiving long-term oxygen therapy (LTOT) or non-invasive ventilation therapy (NIV)
* Subjects with obstructive sleep apnea who are indicated for continuous positive airway pressure (CPAP)
* Subjects with severe complications such as cardiovascular disease, liver disease, renal disease, malignancy, and neurological disease.
Primary outcome measure(s)
- Relationship between sleep time at study enrollment and onset of sarcopenia during follow-up period — Two years
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| National Hospital Organization Minami Kyoto Hospital | Jōyō | Kyoto | Recruiting |
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05193136 on ClinicalTrials.gov ↗ ← All trials in Japan