Distribution of Mood and Personality Characteristics and Their Influence on Treatment Compliance
NCT ID: NCT07101796
Last Updated: 2025-08-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2024-09-14
2025-08-31
Brief Summary
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Detailed Description
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1. Through the personality, mood, and sleep questionnaires of patients with suspected OSA and planned sleep monitoring, the differences in personality and treatment choices of the OSA population with different personality characteristics and emotional states through follow-up.
2. The above investigation and follow-up of patients in the hospital for ventilator pressure treatment were used to observe the effect of differences in personality characteristics and mood status on ventilator treatment acceptance, stress, and compliance indicators.
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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Obstructive sleep apnea (OSA)
dignosis OSA according to the sleep study (AHI\>=5)
continous positive airway pressure (CPAP)
using CPAP to treat OSA
non-OSA
dignosis OSA according to the sleep study (AHI \<5)
No interventions assigned to this group
Interventions
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continous positive airway pressure (CPAP)
using CPAP to treat OSA
Eligibility Criteria
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Inclusion Criteria
* Suspected OSA based on symptoms such as snoring, waking at night, daytime sleepiness, or requiring OSA screening due to related conditions; or confirmed OSA patients referred for sleep monitoring or CPAP pressure titration.
* Subjects are conscious, utterly independent in behavioral and cognitive ability, and able to answer questions independently;
* The patients gave informed consent to the study and cooperated with relevant treatment and evaluation.
Exclusion Criteria
* No symptoms suggestive of OSA and no need for OSA screening; or patients without confirmed OSA
* lacking full independence in behavior and cognitive ability, unable to answer questions independently
* Patients who did not give informed consent or were unwilling to cooperate with treatment and evaluation
18 Years
70 Years
ALL
No
Sponsors
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Peking University First Hospital
OTHER
Responsible Party
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Jing MA
Principal Investigator,
Principal Investigators
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Jing Ma
Role: PRINCIPAL_INVESTIGATOR
Peking University First Hospital
Locations
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Respiratory Department of Peking University First Hospital
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Jing Ma
Role: primary
Other Identifiers
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2024432
Identifier Type: -
Identifier Source: org_study_id
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