Elastic bandXiaomi Mi Band 4 wearable deviceWalking
Elastic band: Thera-Band® elastic band exercise protocol:
First stage (weeks 1-4): Participants performed leg resistance stretching exercises with a red elastic band. In weeks 1-2, exercises were performed 3 times per week, with 2 sets per session; in weeks 3-4, 3 times per week, with 3 sets per session.
Second stage (weeks 5-8): Participants performed leg resistance stretching exercises with a green elastic band. In weeks 5-6, exercises were performed 3 times per week, with 2 sets per session; in weeks 7-8, 3 times per week, with 3 sets per session.
Third stage (weeks 9-12): Participants performed leg resistance stretching exercises with a blue elastic band. In weeks 9-10, exercises were performed 3 times per week, with 2 sets per session; in weeks 11-12, 3 times per week, with 3 sets per session.
Xiaomi Mi Band 4 wearable device: The Xiaomi Mi Band 4 wearable device has been certified by the National Communications Commission (Certification No. CCAG19LP0080T6). From weeks 1 to 12, participants' daily walking steps were monitored using the Xiaomi Mi Band 4 wearable device.
Walking: Walking exercise plan
Study summary
"Patients were divided into two groups: the experimental group (E group) and the control group (C group). The E group received standard care, walking exercise, and elastic band exercise, and wore a smart bracelet to record walking steps and sleep for three months. During the first month, participants performed walking exercise for 100 minutes per week and used a red elastic band for resistance training. In the second month, walking exercise increased to 150 minutes per week with a green elastic band. In the third month, walking exercise increased to 150-300 minutes per week with a blue elastic band. The C group wore the smart bracelet to record walking steps and sleep for three months. Each group included 34 participants. The study was conducted from September 9, 2021, to December 31, 2025. Exclusion criteria included panic disorder, cognitive impairment, current cancer treatment, angina pectoris or myocardial infarction within the past 3 months, participation in high-intensity rehabilitation exercise, and walking dysfunction. Participants were required to follow the study protocol.
* Assessments\*\*:
* Anxiety and Depression\*\*:Measured using the Chinese version of the Hospital Anxiety and Depression Scale (HADS).
* Dyspnea\*\*:Measured using the Modified Medical Research Council (mMRC) scale.
* Life and Sleep quality\*\*:Measured using the COPD Assessment Test (CAT) and Chinese Version of the Pittsburgh Sleep Quality Index (CPSQI).
Eligibility
Sex
ALL
Min age
40 Years
Max age
100 Years
Healthy volunteers
No
Participants were recruited according to the following criteria.
Inclusion Criteria:
* Inpatients diagnosed with chronic obstructive pulmonary disease (COPD) according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria.
* Age ≥ 40 years.
* Post-bronchodilator FEV₁/FVC ratio \< 70%.
* History of smoking.
* Ability to perform walking exercises.
* Willingness of the patient or a family member to provide written informed consent.
Exclusion Criteria:
* Panic disorder.
* Presence of delirium with inability to cooperate.
* Currently receiving cancer treatment.
* Angina pectoris or myocardial infarction within the past 3 months.
* Currently undergoing high-intensity rehabilitation exercises.
Primary outcome measure(s)
Hospital Anxiety and Depression Scale (HADS) — Patients were assessed before discharge as the baseline, and reassessed at 4, 8, and 12 weeks post-discharge. HADS was used to assess differences between groups and over time. The questionnaire consists of 14 items: 7 for anxiety and 7 for depression. Scores range from 0 to 21 for each subscale, with higher scores indicating greater levels of anxiety and depression.
modified Medical Research Council (mMRC) — Patients were assessed before discharge as the baseline, and reassessed at 4, 8, and 12 weeks post-discharge. The mMRC scale was used to assess differences in dyspnea severity between groups over time. The mMRC is a five-point scale ranging from 0 (least severe) to 4 (most severe), with higher scores indicating greater dyspnea severity.
COPD Assessment Test (CAT) — Patients were assessed before discharge as the baseline, and reassessed at 4, 8, and 12 weeks post-discharge. The COPD Assessment Test (CAT) was used to assess differences between groups over time. The CAT consists of 8 items scored from 0 to 5, yielding a total score of 0 to 40, with higher scores indicating a greater impact of COPD on quality of life.
Chinese Version of the Pittsburgh Sleep Quality Index (CPSQI) — Patients were assessed before discharge as the baseline, and reassessed at 4, 8, and 12 weeks post-discharge. CPSQI was used to assess differences between groups over time. Scores range from 0 to 21, with higher scores indicating poorer sleep quality. A score greater than 5 denotes poor sleep quality.
Six-Minute Walk Test ( 6MWT ) — Patients were assessed before discharge as the baseline, and reassessed at 4, 8, and 12 weeks post-discharge. The six-minute walk test (6MWT) was used to assess differences between groups and over time. It is an important measure of patients' functional exercise capacity.
Trial sites (1)
Facility
City
Region
Status
Taipei Tzu Chi Hospital
New Taipei City
Xindian Dist.
Recruiting
More Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation trials in Taiwan
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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