Effect of Online Exercises for Premenstrual Syndrome on Couple's Stress and Family Function
NCT ID: NCT06370429
Last Updated: 2024-05-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
60 participants
INTERVENTIONAL
2024-05-15
2024-12-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Progressive Muscle Relaxation Exercises on Premenstrual Syndrome
NCT06208670
The Effects Of Relaxation Training In Women With Primary Dysmenorrhea
NCT05328869
Effect of Web-Based Life Style Training and Relaxation Training in Women With Premenstrual Syndrome
NCT06705660
Effect of Progressive Muscle Relaxation Exercise on Primary Dysmenorrhea Menstrual Symptoms and Quality of Life.
NCT05340101
Effect of Massage and Progressive Relaxation Exercises on Primary Dysmenorrhea
NCT04356131
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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 sample of the research will consist of women who meet the inclusion criteria. The number of samples was calculated by the researchers using the Power analysis Power 3.1 package program. The sample calculation was based on the study titled 'The Effect of Progressive Relaxation Exercises on Stress Level, Sleep Quality and Exercise Capacity in Young Adults' in the pre-pandemic period in Turkish culture. 80% power from the study of Oğuz et al (2019); By calculating the sample size at an effect size of 0.82 and an error level of 0.05, it was determined that 20 women each should be included in the intervention and control groups in the study. However, since spouses will also participate in the survey process, considering that there may be losses for women and their spouses, the number of participants in each group was increased by 50% and the sample of the study was composed of a total of 60 (Intervention = 30, Control = 30) participants.
Criteria for inclusion in the study:
1\. Volunteering to participate in the study, 2. Being married and living with his wife 3. Being between the ages of 18-45, 5. The woman's ability to use a mobile phone and/or computer to receive online (Zoom; social media) counseling and listen to exercises, 6. The woman and her husband have a social media., application or e-mail address.
7\. The woman and her husband must be literate 8. 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, 11. Not having undergone bilateral oophorectomy or hysterectomy, 12. Not having been diagnosed with polycystic ovary syndrome, 13. Having no other medical disease in the last six months, 14. Participant who does not use oral contraceptives, 15. Without severe psychosomatic disorder, 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. Wanting to leave the research at any stage of the research,
3. Not participating in the final test,
4. Pregnancy occurs,
5. Receiving breathing exercise consultancy from another consultant during the study period
6. Those who do the relaxation exercises incorrectly according to the Content of the Progressive Relaxation Exercises,
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.
Hypotheses:
H1: There is a difference between the mean stress level scores of women with premenstrual syndrome who take online progressive relaxation exercises and women who do not.
H2: There is a difference between the mean stress level scores of women with premenstrual syndrome who receive online progressive relaxation exercises and the spouses of women who do not.
H3: There is a difference between the mean family functionality score of women with premenstrual syndrome who receive online progressive relaxation exercises and those who do not.
H4: There is a difference between the mean family functionality scores of women with premenstrual syndrome who receive online progressive relaxation exercises and their spouses who do not.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Progressive Relaxation Exercises
Progressive Relaxation Exercises, randomized pretest-posttest
Progressive Relaxation Exercises, randomized pretest-posttest
experimental and control ,a randomized pretest-posttest study to examine
control
Non-intervention
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Progressive Relaxation Exercises, randomized pretest-posttest
experimental and control ,a randomized pretest-posttest study to examine
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Being married and living with his wife
3. Being between the ages of 18-45,
4. The woman's ability to use a mobile phone and/or computer to receive online (Zoom; vs) counseling and listen to exercises,
5. The woman and her husband have a application or e-mail address that can use the googledocs application.
6. The woman and her husband must be literate
7. The woman does not have a hearing problem that would prevent her from understanding the voice recording,
8. Scoring 110 or above on the Premenstrual Syndrome Scale
9. Having regular menstrual cycles for the last six months,
10. Not having undergone bilateral oophorectomy or hysterectomy,
11. Not having been diagnosed with polycystic ovary syndrome,
12. Having no other medical disease in the last six months,
13. Participant who does not use oral contraceptives,
14. Without severe psychosomatic disorder,
15. Not pregnant or breastfeeding,
16. No history of cancer.
17. Those who do not use medical drugs to reduce premenstrual syndrome
18. Those who do not use herbal medicine to reduce premenstrual syndrome
19. Do not practice exercise, yoga, etc. to reduce premenstrual syndrome.
Exclusion Criteria
2. Wanting to leave the research at any stage of the research,
3. Not participating in the final test,
4. Pregnancy occurs,
5. Receiving breathing exercise consultancy from another consultant during the study period
6. Those who do the relaxation exercises incorrectly according to the Content of the Progressive Relaxation Exercises CD,
18 Years
45 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Suleyman Demirel University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ayşe Sevim AKBAY KISA
research assistant
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tuba NU KORKMAZ ASLAN
Role: STUDY_CHAIR
Necmettin Erbakan University
Gazi ÇU Kısa
Role: STUDY_CHAIR
Cukurova University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Suleyman Demirel University
Isparta, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
8743432956-050.99-621064
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.