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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04981197
Other study ID # 13-S-013
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 17, 2013
Est. completion date November 30, 2014

Study information

Verified date July 2021
Source National Yang Ming University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was a parallel, randomized controlled trial with a longitudinal research design. Participants were randomly assigned to either the Baduanjin exercise group or the control group. The Baduanjin exercise group received a 12-week Baduanjin exercise programme. The control group received usual care. Fatigue, sleep quality, psychological distress, quality of life were assessed by a structured questionnaire at baseline, 4 weeks, 8 weeks, and 12 weeks after enrollment.


Description:

This study was a parallel, randomized controlled trial with a longitudinal research design. Participants were randomly assigned to either the Baduanjin exercise group or the control group. Patients in the intervention group underwent a 12-week Baduanjin exercise programme consisting of 12 weeks of Baduanjin exercise, a 35-min Baduanjin exercise demonstration video, a picture-based educational brochure, and a performance record form. The control group received usual care. Fatigue, sleep quality, psychological distress, quality of life were assessed by a structured questionnaire at baseline, 4 weeks, 8 weeks, and 12 weeks after enrollment.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date November 30, 2014
Est. primary completion date November 30, 2014
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - Diagnosed with stable heart failure by a physician according to the New York Heart Association (NYHA) class I and II - Aged 20 years or older - Able to communicate and speak Chinese - Have video devices available to use at home Exclusion Criteria: - Impaired mobility, defined as a limitation in independent, purposeful physical movement of the body or of one or more extremities - Unstable angina or myocardial infarction, unstable serious arrhythmia, unstable structural valvular disease, open-heart surgery, or chronic obstructive pulmonary disease (COPD) - Diagnosis of major depression and cognitive disorders - Unstable vital signs (defined as blood pressure > 180/110 mmHg or < 90/60 mmHg and resting heart rate > 100 beats/min).

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Baduanjin exercise
Patients in the intervention group underwent a 12-week Baduanjin exercise programme consisting of 12 weeks of Baduanjin exercise, a 35-min Baduanjin exercise demonstration video, a picture-based educational brochure, and a performance record form.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
National Yang Ming University Ministry of Science and Technology, Taiwan

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in the modified Piper Fatigue Scale scores Changes from baseline modified Piper Fatigue scale at 4 weeks, 8 weeks, 12 weeks.The shortened modified Piper Fatigue scale is composed of 15 items that measure two domains of fatigue: severity and temporality. Each item is scored from 0 to 3, with a total possible score of 0-45. Higher scores indicate greater fatigue. baseline, 4 week, 8 week, 12 week
Primary Changes in the Minnesota Living with Heart Failure Questionnaire scores Changes from baseline Minnesota Living with Heart Failure Questionnaire at 4 weeks, 8 weeks, 12 weeks.The Minnesota Living with Heart Failure Questionnaire is composed of 21 items. Each item score ranges from 0 to 5. The total possible score ranges from 0 to 105, with higher scores indicating a lower quality of life. baseline, 4 week, 8 week, 12 week
Secondary Changes in the Pittsburgh Sleep Quality Index scores Changes from baseline Pittsburgh Sleep Quality Index at 4 weeks, 8 weeks, 12 weeks.The Pittsburgh Sleep Quality Index is composed of 21 items, 7 dimensions. Each dimension is scored from 0 to 3, with a total possible score of 0-21. Higher scores indicate poor sleep. baseline, 4 week, 8 week, 12 week
Secondary Changes in the Hospital Anxiety and Depression Scale scores Changes from baseline Hospital Anxiety and Depression Scale at 4 weeks, 8 weeks, 12 weeks.The Hospital Anxiety and Depression Scale is composed of 14 items, 2 subscales. Each item is scored from 0 to 3, with a total possible score of 0-21 for each subscale. Higher scores indicate higher anxiety and depression baseline, 4 week, 8 week, 12 week
Secondary Changes in heart rate variability Changes from baseline heart rate variability at 4 weeks, 8 weeks, 12 weeks.The heart rate variability was measured using the "Heart Rate Master ANSWatch® Wrist Physiological Monitor TS-0411Deluxe Advanced" (made in Taiwan) baseline, 4 week, 8 week, 12 week
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