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A Brief Lifestyle Modification Programme in Overweight Subjects With Obstructive Sleep Apnoea - Needs Assessment

A Brief Motivational Enhancement Lifestyle Modification Programme to Reduce Body Weight in Overweight Subjects With OSA: Needs Assessment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04262986
Enrollment
100
Registered
2020-02-10
Start date
2020-05-11
Completion date
2022-12-30
Last updated
2022-04-13

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

Conditions

Obstructive Sleep Apnoea, Overweight

Keywords

Lifestyle modification, Obstructive sleep apnoea, Overweight

Brief summary

Obstructive sleep apnea (OSA) is a common chronic disease and associated with cardiovascular and neurocognitive sequelae. Overweight is a common, reversible risk factor of OSA, and the rapid rise in obesity worldwide may lead to increases in OSA and related adverse health outcomes. Weight-loss interventions, especially comprehensive lifestyle interventions, are associated with improvements in OSA severity, cardiometabolic comorbidities, and quality of life. However, the intensive nature of these programmes often pose a barrier to adherence. Furthermore, although there is strong evidence to support the value of mobile text messaging to promote physical activity and healthy eating in clinical and community settings, messaging has rarely been applied in interventions for overweight OSA subjects. The proposed study aims to examine the feasibility of a brief lifestyle modification programme that makes use of smartphone technology (WhatsApp or WeChat) to empower subjects to start doing simple and easy-to-do exercises that can be easily integrated into daily life for gradual lifestyle change.

Detailed description

Obstructive sleep apnea (OSA) is a common chronic disease and associated with cardiovascular and neurocognitive sequelae. Overweight is a common, reversible risk factor of OSA, and the rapid rise in obesity worldwide may lead to increases in OSA and related adverse health outcomes. Weight-loss interventions, especially comprehensive lifestyle interventions, are associated with improvements in OSA severity, cardiometabolic comorbidities, and quality of life. However, non-adherence is commonly seen in such lifestyle modification programmes. Such programmes are often intensive and pose a barrier to adherence. Researchers have suggested that programmes with fewer sessions may improve the completion rates. As yet, there have been no randomised trial assessing the feasibility and effectiveness of a brief theory-based lifestyle modification programme. Furthermore, although there is strong evidence to support the value of mobile text messaging to promote physical activity and healthy eating in clinical and community settings, messaging has rarely been applied in interventions for overweight OSA subjects. In Hong Kong, where smartphone penetration is extensive (89% in 2017), utilising messaging as an intervention tool may be especially valuable. The proposed study will examine the perceived burden and informational needs and preferences of overweight subjects with OSA, especially in relation to physical activity. The study will also examine the feasibility of a brief lifestyle modification programme that makes use of smartphone technology (WhatsApp or WeChat) to provide personalised support and empower subjects to start doing simple and easy-to-do exercises that can be easily integrated into daily life for gradual lifestyle change and weight reduction.

Interventions

None listed

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 years or above; * Performed sleep test in sleep laboratory; and * Mentally fit to provide informed consent and answer self-administered questionnaire.

Exclusion criteria

* Those on CPAP or oral appliance treatment; * Diagnosed with psychiatric illness; or * Unwilling to give informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Preference on physical activityImmediately after obtaining written consentOutcome-based questions with categorical choices

Secondary

MeasureTime frameDescription
Preference on programme contents and informationImmediately after obtaining written consentOutcome-based questions with categorical choices
Preference on m-Health informationImmediately after obtaining written consentOutcome-based questions with categorical choices
Current physical activity practicesImmediately after obtaining written consentOutcome-based questions with categorical choices
Sleep qualityImmediately after obtaining written consentA single-item sleep quality scale; range from 0 -10; Higher score is interpreted as better sleep quality
Dietary consumption habitsImmediately after obtaining written consentOutcome-based questions with categorical choices
Daytime SleepinessImmediately after obtaining written consentEpworth Sleepiness Scale, ranged from 0 - 24 scores. The ESS score (the sum of 8 item scores, 0-3) can range from 0 to 24. The higher the ESS score, the higher that person's average sleep propensity in daily life. Score \>10 is interpreted as excessive daytime sleepiness

Countries

Hong Kong

Contacts

Primary ContactAgnes YK Lai, PhD
agneslai@hku.hk(+852)3917-6328
Backup ContactMary Ip, MD
msmip@hku.hk(+852)2255-4455

Outcome results

None listed

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