- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04346979
Telerehabilitation-based Yoga and Mindfulness Home Program in Postmenopausal Women Having Social Isolation
September 15, 2022 updated by: Yasemin Çırak, Istinye University
The Effect of Telerehabilitation Based Yoga and Mindfulness Home Program on Psychological Resilience, Body Awareness and Physical Activity in Postmenopausal Women Having Social Isolation
In the postmenopausal period when the woman spent 1/3 of her life; Due to the lack of estrogen, some physical and psychological changes occur.
These changes may cause some problems.
For women who perceive menopause as the first step of old age, loss of physical strength, energy, attraction and fertility, menopause can also lead to anxiety.
In addition to these, they are among the emotional changes in the menopausal period in symptoms such as hypersensitivity to events, fatigue, and insomnia.
Sometimes it can even be seen in psychological disorders such as melancholy and depression.
The new coronavirus pneumonia (COVID-19), which appeared in Wuhan in December 2019, started to appear in different countries soon after.
All countries have taken measures to prevent the spread of this virus.
To this end, Turkey remains at home on March 21, 2020, and has commissioned social isolation measures.
Studies investigating the effects of social isolation show that psychological and physical problems occur in individuals.
Studies have shown that yoga and mindfulness programs have an impact on people's anxiety, depression, and the ability to control themselves.
The purpose of this study; To investigate the effectiveness of telerehabilitation based yoga and mindfulness programs on psychological resilience, physical awareness and physical activity in postmenopausal women in social isolation due to the COVID-19 outbreak.
Using telerehabilitation-based home programs aims to use an innovative model.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
50
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
- Istinye 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
45 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Being physically or perceptually competent to exercise,
- No spinal pathology or deformity,
- Volunteering to participate in the study,
- Not having menstruation for at least 12 months
- Hormonally, surgically induced or natural menopause-confirmed women
Exclusion Criteria:
- Those with serious heart disease (aortic stenosis, angina, hypertrophic cardiac myopathy, arrhythmia, pacemaker)
- Those with inflammatory or systemic disease malignancy
- Psychological dysfunction
- Those who use corticosteroids
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study Group
Telerehabilitation based yoga and mindfulness training will be given to the study group.
|
25 volunteers postmenopausal women who are at home during the social isolation process due to the coronavirus outbreak will be included in this group.
Online yoga and mindfulness protocol was created for individuals who will participate in the study.
Each training protocol was planned as 30 minutes for 3 days a week for 6 weeks.
It was planned to start the protocol with warm-up exercises and finish with cooling exercises.
Respiratory exercise was added to the training protocol.
Individuals were asked to participate in the study via telerehabilitation system and aimed to do their exercises with a physiotherapist.
|
|
Experimental: Control Group
Yoga and mindfulness training will be provided by sending a video recording to the control group.
|
25 volunteers postmenopausal women who are at home during the social isolation process due to the coronavirus outbreak will be included in this group.
Online yoga and mindfulness protocol was created for individuals who will participate in the study.
Each training protocol was planned as 30 minutes for 3 days a week for 6 weeks.
It was planned to start the protocol with warm-up exercises and finish with cooling exercises.
The respiratory exercise was added to the training protocol.
Video recordings containing only yoga and mindfulness training were sent to individuals.
The participants were supervised by the researcher.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Brief Resilience Scale
Time Frame: 2 week
|
The scale was used to measure the psychological resilience of individuals and Smith et al. (2008) were developed by.
It is a 5-point Likert type, 6-item self-reporting style measurement tool.
After the items in the scale and reverse coded are translated, the high scores indicate high psychological soundness.
|
2 week
|
|
Nottingham Health Profile
Time Frame: 2 week
|
Nottingham Health Profile was created in England in 1985 to evaluate the quality of life-related to health.
The Nottingham Health Profile is a general quality of life questionnaire that assesses the level of individuals health problems and how they affect their daily life activities.
|
2 week
|
|
Mindful Attention Awareness Scale
Time Frame: 2 week
|
Mindful Attention Awareness Scale developed by Brown and Ryan (2003) is a 15-item scale that measures the general tendency to be aware of and be mindful of instant experiences in daily life.
It has a single factor structure and gives a single total score.
High scores from the scale indicate that conscious awareness is high.
It is a 6-point Likert type scale.
|
2 week
|
|
The Body Awareness Questionnaire
Time Frame: 2 week
|
It is a questionnaire consisting of four subgroups (changes in body process, sleep-wake cycle, prediction at the onset of the disease, prediction of body responses) and a total of 18 expressions aimed at determining the normal or abnormal sensitivity level of the body composition.
The participant is asked to score from one to seven figures for each statement.
In the survey, the ratings are made as total points.
A high score indicates that body sensitivity is better.
|
2 week
|
|
Richard-Campbell Sleep Questionnaire
Time Frame: 2 week
|
It, developed by Richards in 1987, is a 6-item scale that evaluates the depth of night sleep, falling asleep, frequency of waking, awakening when awakened, the quality of sleep and the level of noise in the environment.
Each item is evaluated on the chart between 0 and 100 with a visual analog scale technique.
"0-25" score obtained from the scale indicates very poor sleep, and the "76-100" score indicates very good sleep.
Scale total score is evaluated over 5 items, and item 6 evaluating the noise level in the environment is excluded from the total score assessment.
As the score of the scale increases, the sleep quality of the patients also increases.
|
2 week
|
|
Lateral bridge test
Time Frame: 2 week
|
The participant, who is on the non-dominant side, will be asked to create a support surface from the elbow with the lower arm, place the other hand on the waist, and build a bridge by lifting the hip and knee.
The time that the balance is maintained will be recorded.
|
2 week
|
|
Functional reach test
Time Frame: 2 week
|
It is applied functionally both for the balance of the individual and for measuring the amount of dynamic reach.
The individual is asked to lie down as long as he/she can lie down without going over the heel and hip flexion.
|
2 week
|
|
Beck Depression Scale
Time Frame: 2 week
|
It consists of 21 questions used to evaluate the emotional situation.
Each question is graded between 0-3 and a high score indicates that depressive symptoms increase.
10-16 points indicate mild depressive symptoms, 17-29 points indicate moderate depressive symptoms and 30-63 points indicate severe depressive symptoms.
|
2 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
August 1, 2020
Primary Completion (Actual)
October 1, 2020
Study Completion (Actual)
November 1, 2020
Study Registration Dates
First Submitted
April 13, 2020
First Submitted That Met QC Criteria
April 14, 2020
First Posted (Actual)
April 15, 2020
Study Record Updates
Last Update Posted (Actual)
September 16, 2022
Last Update Submitted That Met QC Criteria
September 15, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 0001 (Researcher)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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