Effect of Online Exercises for Premenstrual Syndrome on Couple's Stress and Family Function (NCT06370429) | Clinical Trial Compass
UnknownNot Applicable
Effect of Online Exercises for Premenstrual Syndrome on Couple's Stress and Family Function
Turkey (Türkiye)60 participantsStarted 2024-05-15
Plain-language summary
Universe of Research The universe of the research; It will consist of women and their spouses with premenstrual syndrome complaints who use social media.
3.6. Sample of the Research The number of samples of the study was composed of a total of 60 (Intervention = 30, Control = 30) participants.
Criteria for inclusion in the study:
* Being married and living with his wife
* Being between the ages of 18-45,
* The woman's ability to use a mobile phone and/or computer to receive online
* The woman and her husband must be literate
* The woman does not have a hearing problem that would prevent her from understanding the voice recording, 9. Scoring 110 or above on the Premenstrual Syndrome Scale 10. Having regular menstrual cycles for the last six months, 13. Having no other medical disease in the last six months, 14. Participant who does not use oral contraceptives, 16. Not pregnant or breastfeeding, 17. No history of cancer. 18. Those who do not use medical drugs to reduce premenstrual syndrome 19. Those who do not use herbal medicine to reduce premenstrual syndrome 20. Do not practice exercise, yoga, etc. to reduce premenstrual syndrome.
Exclusion criteria from the study:
1. He or his spouse fills out the research survey forms incompletely,
2. Pregnancy occurs,
3. Receiving breathing exercise consultancy from another consultant during the study period
Data Collection Method and Duration Descriptive Characteristics Data Form, Perceived Stress Scale (PSS) and Family Assessment Scale will be applied to the sampled women and their spouses. Data collection will continue until the calculated sample number is reached.
Who can participate
Age range
18 Years – 45 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Volunteering to participate in the study,
. Being married and living with his wife
. Being between the ages of 18-45,
. The woman's ability to use a mobile phone and/or computer to receive online (Zoom; vs) counseling and listen to exercises,
. The woman and her husband have a application or e-mail address that can use the googledocs application.
. The woman and her husband must be literate
. The woman does not have a hearing problem that would prevent her from understanding the voice recording,
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Premenstrual Syndrome Scale
Timeframe: The research period for a participant takes approximately 3 months.
2
Family Assessment Scale
Timeframe: The research period for a participant takes approximately four months.
3
Perceived Stress Scale
Timeframe: The research period for a participant takes approximately four months.