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Personalised Active Self-management of Sleep Apnea Program

Key facts

Who runs it
Hong Kong Metropolitan University
Where
Hong Kong1 site in 1 countryChoose a country to see its sites
Trial code
Status
Not yet recruiting
People taking part
60 people, planned
Started
3 Aug 2026
Expected to end
30 Jun 2027
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • 4-month Personalized and Adaptive Sleep Support program (PASS)
  • Control group
Record updated
6 August 2026

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 11 criteriaShow less

Who can take part

  • Aged 18 years and above
  • Newly diagnosed with OSA (diagnosis made within the past year)
  • Newly started or not yet started Positive Airway Pressure (PAP) treatment, with a treatment duration of less than 6 months
  • Physically inactive (self-reported moderate physical activity per week of <150 minutes)
  • Overweight (BMI≥23 kg/m2)
  • Mentally, cognitively, and physically fit to join the trial as determined by the doctor in charge and responsible clinical investigators
  • Able to speak, read, and write Chinese
  • Willing to complete the questionnaires and assessments
  • Has a smartphone

Who cannot take part

  • Use of prescription drugs or clinically significant drugs affecting sleep
  • Clinically significant psychiatric disorder

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

This study is to assess the feasibility and acceptability of the PASS in patients with OSA. Second, the study examines its effectiveness in improving PAP uptake and adherence, self-efficacy in self-care, changes in health-related habits, and health outcomes. We also assess the facilitators and barriers to implementing the PASS.

Read full original descriptionShow less

This is a two-group pilot randomized controlled trial (n=60) with a 4-month follow-up. Subjects assigned to the intervention group will receive a 4-month Personalized and Adaptive Sleep Support (PASS) program, a digital platform-based intervention. The 4-month program incorporates: i) a 20-minute brief motivational interviewing session; ii) a digital platform where users can view personalized OSA health-related videos and information, track their adherence to prescribed treatments, log their daily activities and dietary intake, and set personal health goals; and iii) continuous personalized chat-based messaging and phone call support. Participants in the control group will receive a 4-month general hygiene program, including (i) a 20-minute session, (ii) messaging, and (iii) phone call support.

The feasibility and acceptability of the PASS will be evaluated via semi-structured interviews at the 4-month follow-up. Self-administered questionnaires will be used at baseline and 4 months, and objective assessment tools (such as sleep tests) will be used at baseline and at the 4-month follow-ups. PAP adherence data will be downloaded from PAP machines (if available) for all subjects in both groups at baseline and at month 4.

The 2 groups in the trial

  • General Hygiene Control groupExisting treatment, for comparison

    Participants will receive a 4-month general hygiene information.

    Treatment: Control group

  • PASS Intervention groupTreatment being tested

    Subjects in this arm will receive a 4-month digital Personalized and Adaptive Sleep Support program (PASS).

    Treatment: 4-month Personalized and Adaptive Sleep Support program (PASS)

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
A Personalised Active Self-management of Sleep Apnea Program (PASS) to Improve Positive Airway Pressure Treatment Uptake and Adherence: A Pilot Randomized Controlled Trial
Record updated
6 August 2026