CClinicalTrials.gg
CompletedNCT07382947Updated Feb 3, 2026

MENSTRUATİON MANAGEMENT ACCORDİNG TO GENERATİONS

An interventional study of survey data entry in Menstrual Management, Generational Differences and Womens Health, sponsored by Batman University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2026-02-03.

Sponsored by Batman University · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
1,200
Allocation
Non-randomized
Ages
18 Years to 55 Years
Sex
Female
01

Study summary

The most common symptom that occurs during the menstrual cycle is cramping pain in the lower abdomen. This pain during the menstrual cycle is called dysmenorrhea. It is one of the most common causes of pelvic pain in women. Dysmenorrhea is categorized into two types: primary and secondary. Primary dysmenorrhea manifests as painful cramps during the menstrual period without a pelvic pathology. The pain can radiate to the lower back, pelvis, and upper thigh. Although the etiology of primary dysmenorrhea is not fully known, four main causes have been identified. The etiology of primary dysmenorrhea is endocrine causes, increased prostaglandin levels, increased uterine activity, and psychological causes. Among these factors, increased uterine contractions are thought to be particularly effective in causing the pain. Ischemia in the uterus, which occurs with increased contractions, is among the factors that increase the pain. Primary dysmenorrhea has a prevalence ranging from 45% to 95%. Secondary dysmenorrhea, on the other hand, results from underlying pathological causes such as endometriosis, adenomyosis, uterine fibroids, or pelvic infections. Common symptoms of dysmenorrhea include lower abdominal pain along with headache, numbness, sleep disturbances, depression, vomiting, tender breasts, nausea, diarrhea, and increased urine output.

Read the detailed description

Research objective/rational: The menstrual cycle (MCC) is a physiological process lasting 23-35 days, consisting of two main phases: follicular (from menstruation to ovulation) and luteal (from ovulation to menstruation), characterized by regular fluctuations in estrogen and progesterone hormones. During the menstrual period, estrogen and progesterone levels are low, while in the follicular phase, estrogen increases and peaks at ovulation; at this time, the increase in FSH and LH triggers ovulation. In the luteal phase, progesterone levels rise and peak in the mid-luteal phase, while a second increase in estrogen levels is observed. When fertilization does not occur, both hormones rapidly decrease in the premenstrual period. Mood changes along with these hormonal fluctuations; negative mood increases during the premenstrual and menstrual periods, while positive mood increases during the ovulation period. These changes can negatively affect women's physical activities, work performance, social relationships, and quality of life. The literature reports that women lose more workdays due to health reasons compared to men, and one of the important reasons for this is symptoms associated with the menstrual cycle.

02

Conditions studied

  • Menstrual Management
  • Generational Differences
  • Womens Health
  • Menstrual Health

Keywords

  • menstrual management
  • generational differences
  • womens health
  • menstrual health
03

In context

Lead sponsor

Batman University is the lead sponsor of 13 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Being female
  • Being between 18-55 years of age
  • Having a menstrual cycle
  • Voluntarily agreeing to participate in the study
  • Approving the informed consent form

Exclusion criteria

Exclusion Criteria:

  • Having a serious chronic or neurological disease
  • Using hormonal treatment or birth control method (within the last 6 months)
  • Being pregnant or in menopause
  • Having an incomplete or incorrectly completed questionnaire
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,200 participants (actual)

Study arms

  • Active comparator
    X generation

    Data will be collected online (Google Forms) on a voluntary basis. At the beginning of the survey, participants will be presented with the purpose of the research, privacy principles, and an informed consent form.

    Other: survey data entry

  • Active comparator
    Y Generation

    Data will be collected online (Google Forms) on a voluntary basis. At the beginning of the survey, participants will be presented with the purpose of the research, privacy principles, and an informed consent form.

    Other: survey data entry

  • Active comparator
    Z Generation

    Data will be collected online (Google Forms) on a voluntary basis. At the beginning of the survey, participants will be presented with the purpose of the research, privacy principles, and an informed consent form.

    Other: survey data entry

Interventions

  • Othersurvey data entry

    survey data entry

06

What researchers measure

Primary outcomes

  1. Menstruation Symptom Scale (MSQ)

    Developed by Chesney and Tasto in 1975, the MSQ was adapted into Turkish by Güvenç et al. in 2014. The scale is a five-point Likert-type scale consisting of 22 items. Participants rate menstruation-related symptoms on a scale of 1 (never) to 5 (always). The scale is divided into three sub-dimensions: 'Negative Effects/Somatic Complaints', 'Menstrual Pain Symptoms', and 'Coping Mechanisms'. The MSQ score is calculated from the average scores of the items, and a higher score indicates an increase in the severity of symptoms.

    Time frame: 15 minute

  2. Attitude Toward Menstrution Scale:

    Attitude Toward Menstruation Scale: The Turkish validity and reliability study of the scale developed by Brooks-Gunn and Ruble in 1980 was conducted by Kulakaç et al. in 2008. The adapted version of the scale, which is originally a 7-point Likert type, is a 5-point Likert type with a scoring range of 1-5 (1-Strongly disagree, 5-Strongly agree). The scale, which contains a total of 31 items, has 5 sub-dimensions: "Menstruation as a debilitating event" (7 items), "Menstruation as a disturbing event" (5 items), "Menstruation as a natural event" (5 items), "Noticing/sensing changes before and during menstruation" (8 items), "Denial of the effects of menstruation" (6 items). A high average score on the sub-dimensions or the entire scale indicates a "positive" attitude towards menstruation.

    Time frame: 15 minute

  3. WaLIDD (Working ability, Location, Intensity, Days of pain, Dysmenorrhea) Scale:

    It was first developed by Teherán et al. (2013) and is designed to assess the severity, duration, location, and impact on daily life of dysmenorrhea (menstrual pain) in women. The Turkish adaptation of the scale was carried out by H. Arıkan and E. Erol and published in 2025.

    Time frame: 5 minute

  4. Visual Analog Scale (VAS):

    The Visual Analog Scale (VAS) was used to subjectively determine the pain of the individuals participating in the study. Participants will be asked to indicate the intensity of their pain on a 0-10 cm scale. 1-3 cm will be considered mild, 4-7 cm moderate, and 8-10 cm severe tension.

    Time frame: 1 minute

  5. Turkish Health Literacy Scale (TSOY-32):

    It is a scale developed to measure individuals' ability to find, understand, evaluate, and use health information. It was adapted to the Turkish society by Abacıgil, Harlak, and Okyay (2016), based on the European Health Literacy Scale (HLS-EU-Q47). The scale, consisting of a total of 32 items, evaluates in three main areas: health services, disease prevention, and health promotion. In the validity and reliability analyses, Cronbach's α value was found to be 0.89.

    Time frame: 5 minute

  6. Step Count:

    The WHO defines mobile health as the support of medical and public health applications by mobile devices such as mobile phones, patient monitoring devices, and other wireless devices. Mobile phones are the most commonly used devices in the implementation of mobile health (WHO, 2011). Many studies have reported that pedometers installed on smartphones provide accurate step counting at different walking speeds and with different carrying methods (Funk et al., 2018; Thomson et al., 2019). A-B Participants' physical activity levels were monitored for 7 days through the Google Fit application installed on smartphones. The application automatically records the daily step count, distance covered, and estimated energy expenditure using the device's accelerometer sensor. Participants were asked to keep their phones on them throughout the day and to keep the application open in the background. The average daily step count obtained at the end of 7 days was evaluated as an indicator o

    Time frame: 1 minute

  7. Pittsburgh Sleep Quality Index (PSQI):

    Developed by Buysse and colleagues in 1989, the PSQI is a self-report questionnaire that assesses sleep quality and disturbances over the past month. A validity and reliability study conducted in Turkey by Ağargün and colleagues proved that the PSQI is consistent and valid in Turkish society. This scale, consisting of 24 questions, comprises 19 questions based on the individual's self-assessment and 5 questions answered by a spouse or roommate. Each question is scored between 0 and 3 to calculate the total score. A score of five or higher is generally considered poor sleep quality.

    Time frame: 5 minute

  8. Short Form-12 (SF-12):

    Participants' health-related quality of life was assessed using the Short Form-12 (SF-12) scale. SF-12 is a short questionnaire consisting of two sub-dimensions, physical and mental health, measuring participants' general health status and quality of life. The physical component score (Physical Component Summary, PCS) and the mental component score (Mental Component Summary, MCS) were calculated separately, with higher scores indicating better quality of life. The Turkish validity and reliability of the scale were established by Demiral et al. (2006).

    Time frame: 5 minute

07

Study locations

1 site
  • Batman Center
    Batman, Gültepe 72000, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07382947
Lead sponsor
Batman University
Responsible party
merve yiğit kocamer (DR, Batman University) — Principal investigator
First posted
Feb 3, 2026
Start date
Nov 1, 2025
Primary completion
Jan 10, 2026
Completion
Jan 10, 2026
Last update
Feb 3, 2026

Study contacts

merve yiğit kocamer, lecturer
principal investigator · Batman University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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