The Effect of Education Given According to the Health Promotion Model on Premenstrual Symptoms, Emotional Eating Behavior and Perceived Stress
NCT ID: NCT06105567
Last Updated: 2025-02-10
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
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COMPLETED
NA
86 participants
INTERVENTIONAL
2023-10-30
2024-10-07
Brief Summary
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In this study, it is thought that the training given according to the health promotion model will both create a resource for nurses and contribute to the literature with the results obtained by applying this training to people experiencing PMS.The research will be conducted as a pretest-posttest randomized controlled study.
H1: Education given according to the health promotion model has an effect on premenstrual symptoms, emotional eating behavior and perceived stress.
H0: Education given according to the health promotion model has no effect on premenstrual symptoms, emotional eating behavior and perceived stress.
The total number of students in the research population is 330.In the G\*Power 3.1.9.7 program, for the effect size t test, d = 0.94, alpha (α) = 0.05, and power (1-β) = 0.95, and the minimum total sample number was determined as 52, experimental group: 26, control group: 26. . However, taking into account the losses in the study, a total of 60 people will be included in the study. (experiment:30, control:30).
The first group will be divided into the group trained according to the health promotion model using the Philips 66 technique, and the second group will be divided into the control group.
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Detailed Description
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H1: Education given according to the health promotion model has an effect on premenstrual symptoms, emotional eating behavior and perceived stress.
H0: Education given according to the health promotion model has no effect on premenstrual symptoms, emotional eating behavior and perceived stress.
The total number of students in the research population is 330.In the G\*Power 3.1.9.7 program, for the effect size t test, d = 0.94, alpha (α) = 0.05, and power (1-β) = 0.95, and the minimum total sample number was determined as 52, experimental group: 26, control group: 26. . However, taking into account the losses in the study, a total of 60 people will be included in the study. (experiment:30, control:30).
The first group will be divided into the group trained according to the health promotion model using the Philips 66 technique, and the second group will be divided into the control group.In the first stage, the "Premenstrual Syndrome Scale" will be applied to the students and the students will be placed in the experimental and control groups. In the second stage, Personal Information Form, PMS Scale, Premenstrual Eating Habits Form, Healthy Lifestyle Behaviors Scale, Emotional Eating Scale, Perceived Stress Scale and Visual Vissual Pain Scale will be applied to the students in this group before training. Data will be collected by face-to-face research method. Premenstrual syndrome periods will be determined by creating a menstrual cycle calendar for the participants. In the third stage, students in the experimental group will be trained with the first powerpoint presentation. Then brochures will be distributed. It will be applied according to the Philips 66 technique. In the fourth stage, 4 weeks after the first training, general reminder training will be given online during students' pms periods. In the fifth stage, 4 weeks after the second training, survey forms will be filled out by the experimental group and the control group.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Effect of Education on Premenstrual Symptoms, Emotional Eating Behavior and Perceived Stress
Students who score over 110 on the premenstrual syndrome scale and meet the study criteria will be included in the experimental and control groups. Personal Information Form, PMS Scale, Premenstrual Eating Habits Form, Healthy Lifestyle Behaviors Scale, Emotional Eating Scale, Perceived Stress Scale and Visual Visual Pain Scale will be administered to the students in this group before the training. Premenstrual syndrome periods will be determined by creating a menstrual cycle calendar for the participants. Students will be trained with their first powerpoint presentation. Afterwards, brochures will be distributed. It will be applied according to the Philips 66 technique. 4 weeks after the first training, students will be given general reminder training online during pms periods. Survey forms will be filled out by the group 4 weeks after the second training.
Training given according to the health promotion model by applying the Philips 66 technique
The Effect of Education Given According to the Health Promotion Model on Premenstrual Symptoms, Emotional Eating Behavior and Perceived Stress
control group
Students who score over 110 on the premenstrual syndrome scale and meet the study criteria will be included in the experimental and control groups. Students in this group will not receive training and will be administered the Personal Information Form, PMS Scale, Premenstrual Eating Habits Form, Healthy Lifestyle Behaviors Scale, Emotional Eating Scale, Perceived Stress Scale and Visual Vissual Pain Scale. Data will be collected by face-to-face research method. Survey forms will be filled out by the control group.
No interventions assigned to this group
Interventions
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Training given according to the health promotion model by applying the Philips 66 technique
The Effect of Education Given According to the Health Promotion Model on Premenstrual Symptoms, Emotional Eating Behavior and Perceived Stress
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Experiencing at least five PMS symptoms every month,
* Not having had sexual intercourse
* Regular menstruation, (regular menstruation (between 21-35 days))
* Not having any chronic disease,
* Not using any method to cope with PMS
* Not taking Hormone Replacement Therapy
* Women who agreed to participate in the study were included in the study group.
Exclusion Criteria
* Allergy,
* Irregular menstruation,
* Not having regular menstrual periods in the last three months,
* Having received a psychiatric diagnosis,
* Do not have any gynecological disease (abnormal uterine bleeding, myoma, ovarian cyst, etc.)
* Using contraceptive medication,
* 1st and 4th year nursing and midwifery students
18 Years
30 Years
FEMALE
No
Sponsors
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Kafkas University
OTHER
Responsible Party
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Cansu Mine Aydin
research assistant
Locations
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Kafkas University
Kars, Kars, Turkey (Türkiye)
Countries
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Other Identifiers
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KAFKAS-SAG-CMAYDIN-002
Identifier Type: -
Identifier Source: org_study_id
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