Comparison of Qigong Exercises on Two Different Digital Platforms

November 17, 2021 updated by: Buket AKINCI, Biruni University

Comparison of Qigong Exercises on Two Different Digital Platforms: an Evaluation Project of Technologically Supported Activity

Mild effort requiring, body-mind oriented, effective on multiple physical fitness parameters, ancient exercise method Qigong would be beneficial for a great number of people by using popular technological mediums in order to increase overall physical activity and wellbeing. Our aim is to evaluate the effects of Qigong exercises on endurance, muscle strength, sleep quality, level of anxiety and stress by using two different tele-rehabilitation methods.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Physical inactivity and sedentary behavior is a serious public health problem which categorized as a pandemic. One of the common risk factors for cardiovascular diseases, cancers, chronic respiratory diseases and diabetes, known as chronic non-communicable diseases, is physical inactivity. Mild effort requiring, body-mind oriented, effective on multiple physical fitness parameters, ancient exercise method Qigong would be beneficial for a great number of people by using popular technological mediums in order to increase overall physical activity and wellbeing. Based on reasons as previously described, our aim is to evaluate the effects of Qigong exercises on endurance, muscle strength, sleep quality, level of anxiety and stress by using two different tele-rehabilitation methods.

Study Type

Interventional

Enrollment (Actual)

32

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Biruni University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • • Categorized as "inactive (<600 metabolic equivalent-min/hf)" with respect to International Physical Activity Questionnaire

    • Ability to read and talk in Turkish
    • In order to join online sessions, participants should have internet access
    • All answers of the Physical Activity Preparation Survey should be selected as "No"

Exclusion Criteria:

  • • Lack of cooperation

    • Uncontrolled hypertension and uncontrolled arrhythmia patience
    • People with serious neurological and respiratory conditions
    • Having a pacemaker and/or percutaneous transluminal coronary angioplasty
    • Stroke, myocardial infarction history
    • Amputee
    • People with serious major musculoskeletal problems
    • Chronic kidney failure
    • Chronic Liver failure
    • Hip or knee prosthesis in last five years
    • Lower extremity injuries in last 6 months
    • Diabetic ulcer or neuropathy
    • Pregnant or planning to get pregnant in 1 year
    • Breastfeeding
    • Taking sleep pills or taking medicines as part of psychological treatment and/or working on shifts

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1=Video-conference based Qigong exercises
After initial result evaluation, participants of Group A will perform Qigong exercises for 40 to 45 minutes per session for 3 days a week for 6 weeks via the online video conference method.
Specific Qigong exercises 1- Painting the rainbow 2-Raising the arms 3-Looking at the moon 4- Pushing the waves
Experimental: Group 2=A-synchronized video Qigong exercises

Group B will perform the same routine via a-synchronized video sections for 6 weeks.

Basic Qigong exercises will be performed by volunteers for 6 weeks and progression will be logged.

Specific Qigong exercises 1- Painting the rainbow 2-Raising the arms 3-Looking at the moon 4- Pushing the waves

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
International Physical Activity Questionnaire-Short form
Time Frame: 8 weeks
Determines the physical activity level of the participants
8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
1 Minute Sit-Stand Test
Time Frame: 8 weeks
Determines the functional mobility and lower extremity levels
8 weeks
Pittsburgh Sleep Quality Index
Time Frame: 8 weeks
Determines the sleep quality of participants
8 weeks
Coronavirus Anxiety Index
Time Frame: 8 weeks
Determines the coronavirus anxiety
8 weeks
Perceived Stress Index
Time Frame: 8 weeks
Determines the perceived stress
8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Buket AKINCI, Assoc.Prof., Biruni University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 27, 2021

Primary Completion (Actual)

September 1, 2021

Study Completion (Actual)

November 17, 2021

Study Registration Dates

First Submitted

April 20, 2021

First Submitted That Met QC Criteria

April 24, 2021

First Posted (Actual)

April 28, 2021

Study Record Updates

Last Update Posted (Actual)

November 18, 2021

Last Update Submitted That Met QC Criteria

November 17, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 2015-KAEK-47-21-02

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The individual participant data will not be shared

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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