New coaching program aims to boost ventilator use in chronic lung patients
NCT ID NCT05008211
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a 6-week coaching program based on the Information-Motivation-Behavioral skills model to help patients with chronic hypercapnic respiratory failure use their home ventilator more consistently. The program included education, motivation, and practical skills training. 124 patients who were not using their ventilator enough took part. The goal was to see if the program could improve how often and how long they used the ventilator each night.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Information-Motivation-Behavioral skills (IMB) model-based intervention
- What this could lead to
- If successful, this program could help patients with chronic breathing failure use their home ventilator more regularly, potentially reducing hospital visits and improving quality of life.
- What could go wrong
- This is a small, completed study with 124 participants, so results may not apply to everyone. The intervention is behavioral, so individual motivation and circumstances may limit its effectiveness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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124 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * (1) CHRF (i.e., PaCO2 ≥ 7 kPa or 52.5 mmHg) for at least 4 weeks, and * (2) using domiciliary NIV for ≥ 4 weeks, and * (3) non-adherer (i.e., used domiciliary NIV for \< 4 hours per night or \< 70% of days or with a mean daily use \< 5 hours per day in the last 2 weeks) Exclusion Criteria: * (1) known psychiatric disorders except anxiety and depression; or * (2) diseases limiting life expectancy to ≤ one year; or * (3) active malignancy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Department of Medicine and Geriatrics, United Christian Hospital
Hong Kong, Hong Kong
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