Cognitive and Psychomotor Skills and Behavioural Changes During Ramadan in Women (NCT06865014) | Clinical Trial Compass
CompletedNot Applicable
Cognitive and Psychomotor Skills and Behavioural Changes During Ramadan in Women
Turkey (Türkiye)22 participantsStarted 2025-02-23
Plain-language summary
This study will observe the participants fasting during the month ramadan. Descriptive characteristics and assessments of sleep, food consumption, body composition, cognitive skills, anticipation time, and physical activity will be conducted before, during and after ramadan.
Who can participate
Age range
18 Years – 24 Years
Sex
FEMALE
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:
* Voluntariness: Participants must be willing to participate in the study voluntarily and provide informed consent.
* Absence of any health issues
* No chronic sleep problems
* No use of sleep medication
* Fasting throughout the study period during the month Ramadan
Exclusion Criteria:
* Complications During the Intervention: Participants who experience any complications during the month Ramadan while fasting.
* Irregular fasting behavior during Ramadan
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
Actigraphy
Timeframe: Pre-test, following one week first mid-test, following three weeks second mid-test and following two weeks post-test
2
Body weight measurement
Timeframe: Pre-test, following one month mid-test and following another one month post-test
3
Body fat percentage
Timeframe: Pre-test, following one month mid-test and following another one month post-test
4
Food consumption assessment
Timeframe: Pre-test, following one week first mid-test, following three weeks second mid-test and following two weeks post-test
5
Stroop test
Timeframe: Pre-test, following one week first mid-test, following three weeks second mid-test and following two weeks post-test
6
Letter Digit Substitution Test
Timeframe: Pre-test, following one week first mid-test, following three weeks second mid-test and following two weeks post-test