CClinicalTrials.gg
CompletedNCT06532864Updated Oct 1, 2024

Qigong Exercise and Sleep Quality

An interventional study of Practice Mawangdui Guiding Technique in Sleep Quality, sponsored by Hunan University of Traditional Chinese Medicine. Completed at 1 site in China. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2024-10-01.

Sponsored by Hunan University of Traditional Chinese Medicine · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study summary

The purpose of this study was to investigate whether 12 weeks of practicing Mawangdui Guiding Technique has an improvement effect on subjective sleep quality, objective sleep quality, and daytime fatigue in older adults in a healthcare hospital.

02

Conditions studied

  • Sleep Quality

Keywords

  • sleep quality
  • older adults
03

In context

Lead sponsor

Hunan University of Traditional Chinese Medicine is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Aged sixty years and above; continuous residence in the participating healthcare hospitals for more than six months
  • Conscious, with basic visual and auditory perception, communication, and cognitive functioning
  • Voluntary enrollment in this study and signing of the informed consent form.

Exclusion criteria

Exclusion Criteria:

  • Individuals who have suffered a sudden accident, emergency surgery, or a rapid deterioration of a long-term medical condition
  • Individuals who have recently been involved in other rehabilitation activities and who play sports on a regular basis
  • Individuals who are unable to participate in physical activity (e.g., patients suffering from major diseases of the liver, kidneys, heart, brain, or blood system)
  • Individuals suffering from deep venous thrombosis; individuals with musculoskeletal problems with signs of limitation of movement (e.g., unsettled broken bones, pelvic fractures)
  • Individuals with preexisting psychiatric conditions (such as personality disorders, psychosis, and so on); and individuals with symptoms of severe depression.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Practicing Mawangdui Guidance Exersize Group

    The experimental group underwent the Mawangdui Guided Exercise, which consisted of five 45-minute sessions per week for 12 weeks.

    Behavioral: Practice Mawangdui Guiding Technique

  • No intervention
    Sleep Education Group

    The control group maintained routine sleep education in addition to daily activities.

Interventions

  • BehavioralPractice Mawangdui Guiding Technique

    Nursing staff with experience in teaching Mawangdui Daoyin Exercise conducted the operation instruction on different floors. A feasibility assessment of the older adults was carried out by the nursing staff at the end of the teaching, and only after passing this assessment could the experimental part begin. The treatment group participated in five Mawangdui Daoyin Exercise sessions per week, each lasting approximately 45 minutes, and the exercises continued for 12 weeks.

06

What researchers measure

Primary outcomes

  1. Pittsburgh Sleep Quality Index

    The Pittsburgh Sleep Quality Index is a comprehensive sleep self-assessment tool containing 19 items. The overall total score ranges from 0-21, with the lower the overall score, the higher the quality of sleep.

    Time frame: baseline; 4 weeks; 12weeks

  2. Insomnia Severity Index

    The Insomnia Severity Index(ISI) is a self-assessment tool consisting of seven items designed to assess various aspects of insomnia. Cumulative ISI scores range from 0 to 28 and are categorized as follows: 0-7 = no insomnia; 8-14 = mild insomnia; 15-21 = moderate insomnia; and 22-28 = severe insomnia.

    Time frame: baseline; 4 weeks; 12weeks

  3. Polysomnography

    Polysomnography is the internationally recognized gold standard for diagnosing sleep disorder disorders and can provide an objective basis for the diagnosis, classification and identification of sleep disorders.

    Time frame: baseline; 4 weeks; 12weeks

  4. Flinders Fatigue Scale

    The Flinders Fatigue Scale is a 7-item scale that measures various characteristics of fatigue. Total fatigue scores range from 0 to 31, with higher scores indicating more severe fatigue.

    Time frame: baseline; 4 weeks; 12weeks

07

Study locations

1 site
  • Healthcare Hospital
    Changsha, Hunan 410000, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 1, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06532864
Lead sponsor
Hunan University of Traditional Chinese Medicine
Responsible party
Huan Liu (teacher, Hunan University of Traditional Chinese Medicine) — Principal investigator
First posted
Aug 1, 2024
Start date
Jun 1, 2024
Primary completion
Aug 15, 2024
Completion
Aug 20, 2024
Last update
Oct 1, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion