Tiny activity 'Snacks' may sharpen minds in COPD
NCT ID NCT07702994
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study tests a program called Snacktivity, which involves doing very short bursts of moderate exercise—like brisk walking for 2 to 5 minutes, several times a day—to see if it can improve thinking skills and the ability to manage daily health in people aged 60 and older with COPD. Participants wear an activity tracker and follow a guide for 12 weeks. The program is being culturally adapted for people in Hong Kong through workshops with patients, families, and healthcare professionals.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a culturally adapted Snacktivity program of short, moderate-intensity physical activity snacks (2-5 minutes, 5-6 times daily) plus a Garmin activity tracker and self-guided manual
- What this could lead to
- If it works, this could offer a simple, practical way for people with COPD to boost brain function and better manage their own health through brief, frequent physical activity.
- What could go wrong
- This is an early-stage trial testing feasibility and short-term effects, so results may not be definitive. The program requires daily commitment, and benefits may vary by individual.
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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About 210 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- 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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60 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* Inclusion Criteria: 1. Confirmed diagnosis of COPD in accordance with the 2026 Global Initiative for Chronic Obstructive Lung Disease (GOLD) Guideline, with a post-bronchodilator ratio of FEV₁/FVC \< 70%; 2. Aged ≥ 60 years; 3. Clinically stable condition; 4. Score at or below the age- and education-adjusted cutoff (16th percentile) on the Hong Kong Montreal Cognitive Assessment (HK-MoCA) 5-minute Protocol, indicating mild cognitive impairment; 5. No exercise contraindications; 6. No active wrist skin conditions that would prevent wearing an activity tracker (Phase 2 \& 3); 7. Willingness to wear an activity tracker during the intervention (Phase 2 \& 3); 8. Possession of a smartphone capable of receiving instant messages (Phase 2 \& 3); 9. Proficiency in Cantonese or Mandarin; 10. Willingness to provide written informed consent and commitment to trial completion. * Exclusion Criteria 1. Receipt of oxygen therapy for ≥ 15 hours per day or requirement for mechanical ventilation; 2. History of brain injury or stroke; 3. Presence of severe comorbidities including coronary artery disease, severe hepatic or renal dysfunction; 4. Diagnosis of psychiatric disorders, deafness, severely limited physical mobility, or inability to cooperate with trial interventions; 5. For Phase 2 and Phase 3: Use of medications documented to impact cognitive function.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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