Investigating the effectiveness of psychological education of the patient and spouse in people with obstructive sleep apnea following the CPAP device, improving sleep quality and reducing daily sleepiness

Not Applicable

Recruiting

• Conditions: Patients with obstructive sleep apnea.; Sleep apnea; G47.3

• Registration Number: IRCT20240203060885N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

Patients with obstructive sleep apnea
patients who want to use CPAP device
completing questionnaires related to sleep quality and daily sleepiness
marriage

Exclusion Criteria

suffering from severe mental illnesses (psychotic, bipolar)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patients with obstructive sleep apnea who use a CPAP machine. Timepoint: The measurement is done before the start of the intervention, immediately after the end of the intervention and eight weeks after the intervention. Method of measurement: Using the Petersburg Sleep Quality Questionnaire and Epworth Daily Sleepiness Questionnaire.

Secondary Outcome Measures

Name	Time	Method
Improving sleep quality. Timepoint: The measurement is done before the start of the intervention, immediately after the end of the intervention and eight weeks after the intervention. Method of measurement: Using the Petersburg Sleep Quality Questionnaire and the Epworth Daily Sleepiness Questionnaire.;Reducing daily sleepiness. Timepoint: The measurement is done before the start of the intervention, immediately after the end of the intervention and eight weeks after the intervention. Method of measurement: Using the Petersburg Sleep Quality Questionnaire and the Epworth Daily Sleepiness Questionnaire.