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The Effectiveness of Smartphone Application on the Serevity of Obstructive Sleep Apnea

C

Chang Gung University of Science and Technology

Status

Completed

Conditions

Obstructive Sleep Apnea

Treatments

Behavioral: Smartphone Application with lifestyle modification Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05127239
201802318B0A3

Details and patient eligibility

About

A two-year study design is formulated. The overall aim of this study is to examine the effectiveness of the care model combing smartphone application on improve obstructive apnea in obesity adults.

Full description

This study was the second year.The purpose of this study is to evaluate the effectiveness of the lifestyle modification intervention for overweight employees with obstructive sleep apnea. A randomized control trial with single blind will be used. Stratified with proportional randomized sampling will be employed and 160 suitable participants will be recruited from 4 electronics industries in northern of Taiwan. The subjects will be randomly divided into three groups. The total duration of intervention program is 6 months. Only the intervention group received the Combining Smartphone Application with lifestyle modification Intervention. The home portable sleep monitor will be used to collect the change of AHI at baseline, 3, and 6 months after intervention.

Enrollment

146 patients

Sex

All

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: a) >21 years old; b) )BMI greater than24 kg/m2; (c) the absence of any mental disorder, alcohol and drug addiction, and serious disease, such as cancer or cardiorespiratory failure; and d) Screening for OSA , AHI>5 and voluntary participation.

Exclusion Criteria:

  • a) diagnosis of OSA and currently under treatment and;b) diagnosis of severe depression (c) have cardiopulmonary diseases and are not suitable for activities; and d) plan to become pregnant during or within 6 months

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

146 participants in 3 patient groups

smartphone application with education
Experimental group
Description:
participants were provides 3 times lifestyle modification education and using smartphone app program
Treatment:
Behavioral: Smartphone Application with lifestyle modification Intervention
smartphone application
Experimental group
Description:
participants were only provided smartphone app program
Treatment:
Behavioral: Smartphone Application with lifestyle modification Intervention
waiting list
No Intervention group
Description:
No intervention was provided, but researchers explained the results of OSA screening for participants after every examination

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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