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Lifestyle Modification Using an App in OSA

Effect of Lifestyle Modification Using Smartphone Application on Weight Reduction and Obstructive Sleep Apnea

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03189940
Enrollment
59
Registered
2017-06-16
Start date
2016-06-20
Completion date
2016-11-18
Last updated
2017-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Obstructive Sleep Apnea

Brief summary

This study aimed to investigate the effects of a mobile phone app linked to hospital electronic medical record (EMR) system on weight reduction and obstructive sleep apnea (OSA). Adults aged \> 20 years with witnessed snoring or sleep apnea from a sleep clinic of a tertiary center were prospectively enrolled, and the participats were randomized into app user and control groups. The mobile app was designed to collect daily lifestyle data by wearing a wrist activity tracker and reporting dietary intake. At the visit after 2 weeks of use, a summary of the lifestyle was displayed on the hospital EMR and reviewed by both physicians and app users. Further lifestyle modification was encouraged on the basis of the electronically collected data. In the control group, the lifestyle modification performed as the usual practice. All participants underwent Watch PAT and body mass index (BMI) measurement twice: on enrollment; and after 4-weeks follow up. Changes of BMI, and parameters of sleep related breathing were analyzed.

Interventions

BEHAVIORALLife style modification by using and app with a wrist-worn activity tracker

The mobile app was designed to collect daily lifestyle data by wearing a wrist activity tracker and reporting dietary intake. At the visit after 2 weeks of use, a summary of the lifestyle was displayed on the hospital EMR and reviewed by both physicians and app users. Further lifestyle modification was encouraged on the basis of the electronically collected data.

BEHAVIORALConventional Life style modification

Physician's usual consultation for life style modification at 0 week, and 2 weeks of enrollment

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

ᆞ patients must agree to participate in our clinical study ᆞ patients without severe cardiopulmonary disease ᆞ patients must be with BMI \> 23 Kg/m2

Exclusion criteria

ᆞ patients who did not agree ᆞ patients with severe cardiopulmonary disease ᆞpatients who are under treatment using a continuous positive airway pressure device or a mandibular advancement device ᆞ patients who were pregnant

Design outcomes

Primary

MeasureTime frameDescription
changes in body weightbase line and after 4weeks of life style modiciationbody weight measurement and calculate into body mass index (BMI)

Secondary

MeasureTime frameDescription
apnea hypopnea index (AHI)base line and after 4weeks of life style modiciationnumber of apnea and or hypopnea event per hour during sleep
respiratory distress index (RDI)base line and after 4weeks of life style modiciationAHI + number of respiratory effor related arousal (RERA) per hour during sleep
oxygen desaturation index (ODI)base line and after 4weeks of life style modiciationnumber of desaturation event (peripheral oxygen satuation less than 90%) per hour during sleep
sleep time proportion with snoring loudness > 45dBbase line and after 4weeks of life style modiciationtotal duration of the snoring loudness \>45 dB devided by the total sleep time (%)
lowest oxygen saturationbase line and after 4weeks of life style modiciationthe degree of the lowest oxygen saturation measured during sleep

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026