- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04695808
The Effect of Yoga Training on Menopausal Symptoms on Menopausal Women
May 26, 2022 updated by: Arzu Abiç, Eastern Mediterranean University
Parallel to the increase in life expectancy by years, the population of women living in the post-menopausal period is also increasing.
In order to have a healthy menopause, which is an important part of women's life, it is thought that the adoption of yoga practice without health risks by women and its implementation as a lifestyle may be effective in reducing the symptoms of menopause experienced by women.
In line with this information, it is aimed to determine the effect of yoga training on menopausal symptoms.
The research will be carried out with menopausal women between the ages of 40-60 in Famagusta region.
Women will be divided into two groups as intervention and control.
Personal information form and menopause rating scale will be used in the research.
The intervention group will be given yoga practice two days a week for 10 weeks.
Menopause rating scale will be applied to the intervention and control group before and after the research.
Study Overview
Detailed Description
Parallel to the increase in life expectancy by years, the population of women living in the post-menopausal period is also increasing.
In order to have a healthy menopause, which is an important part of women's life, it is thought that the adoption of yoga practice without health risks by women and its implementation as a lifestyle may be effective in reducing the symptoms of menopause experienced by women.
In line with this information, it is aimed to determine the effect of yoga training on menopausal symptoms.
The research will be carried out with menopausal women between the ages of 40-60 in Famagusta region.
Women will be divided into two groups as intervention and control.
Personal information form and menopause rating scale will be used in the research.
The intervention group will be given yoga practice two days a week for 10 weeks.
Menopause rating scale will be applied to the intervention and control group before and after the research.
Study Type
Interventional
Enrollment (Actual)
62
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
-
-
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Famagusta, Cyprus, 90
- Eastern Mediterranean 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
40 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Willing to participate in research,
- Can read and write in Turkish,
- Open to communication,
- Those who are between the ages of 40-60 and do not experience menstruation for at least one year, Do not use medication to treat menopausal symptoms,
- No diagnosed musculoskeletal disease, no severe heart disease,
- Not doing regular exercise and yoga,
- Not surgically menopausal,
- Women without psychiatric problems
Exclusion Criteria:
- Refusing to participate in research,
- Can't read and write Turkish,
- Communication is not possible,
- Those who are younger than 40 or older than 60 have experienced menstruation for at least one year
- Using medication for the treatment of menopausal symptoms,
- Those with a diagnosed musculoskeletal disease, severe heart disease,
- Doing regular exercise and yoga,
- Surgically menopausal, Women with psychiatric problems
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: control group
no intervention
|
|
Experimental: intervention group
Yoga practice will be done two days a week for 10 weeks.
|
Yoga practice will be done two days a week for 10 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
menopause rating scale
Time Frame: 3 months
|
It was developed in German by Schneider et al.
In 1992 to measure the severity of menopausal symptoms and was adapted to English in 1996.
MRT was adapted to Turkish by Gürkan in our country in 2005.
There are "0 = None", "1 = Mild", "2 = Moderate", "3 = Severe" and "4 = Very severe" options for each item in the Likert-type scale consisting of 11 items including menopausal complaints.
The total score of the scale is calculated based on the scores given for each item.
The lowest score that can be obtained from the scale is 0, the highest score is 44.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
- Efficacy of yoga for vasomotor symptoms: a randomized controlled trial
- Efficacy of omega-3 for vasomotor symptoms treatment: a randomized controlled trial
- Hatha Yoga practice decreases menopause symptoms and improves quality of life: A randomized controlled trial
- Effects of Yoga and Aerobic Exercise on Actigraphic Sleep Parameters in Menopausal Women with Hot Flashes
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)
September 15, 2020
Primary Completion (Actual)
October 15, 2020
Study Completion (Actual)
November 29, 2020
Study Registration Dates
First Submitted
December 28, 2020
First Submitted That Met QC Criteria
January 4, 2021
First Posted (Actual)
January 5, 2021
Study Record Updates
Last Update Posted (Actual)
May 27, 2022
Last Update Submitted That Met QC Criteria
May 26, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- g9987n5g
- Duygu Yılmaz Vefikulucay (Other Identifier: Eastern Mediterranean University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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