Not Yet RecruitingNot Applicable

Aerobic Exercises Versus Sub Occipital Myofascial Release on Memory Function in Females With Premenstrual Syndrome.

Egypt40 participantsStarted 2026-07-03

Plain-language summary

This study will be conducted to investigate the effect of aerobic exercises versus sub occipital Myofascial release on memory functions in females with premenstrual syndrome.

Who can participate

Age range

18 Years – 30 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: Females with premenstrual syndrome and memory function deficits have to meet the following criteria in order to participate in this study: * Their age ranged from 18 to 30 years old. * Their body mass index (BMI) ranged from 18.5 - 30 kg/cm2. Exclusion Criteria: * Any medications that can affect central nervous system or memory function. * Any neurological disorders affect their memory function. * Pregnant women. * Daily smokers. * Had a concussion or head trauma within the past 30 days. * Took any illegal drugs or alcohol within the past 30 days.

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

Memory function

Timeframe: 6 weeks

Prospective and retrospective memory questionnaire (PRMQ)

Timeframe: 6 weeks

Trial details

NCT IDNCT07684495

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-09-20

Contact for this trial

Gehad Ali, Bachelor

01140675084 jihad7mohammad7@gmail.com

View on ClinicalTrials.gov More Premenstrual Syndrome trials