Can a jog or a massage sharpen your memory during PMS?
NCT ID NCT07684495
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This study compares two non-drug approaches—aerobic exercise and a specific neck massage technique—to see if they can improve memory in women with premenstrual syndrome (PMS). Researchers will enroll 40 women aged 18 to 30 who have PMS and memory complaints. Participants will be assigned to either a treadmill exercise program or a manual therapy session targeting the neck muscles, and their memory and stress levels will be measured before and after treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Aerobic exercise and suboccipital myofascial release (neck massage)
- What this could lead to
- If effective, this could offer simple, drug-free ways to help with memory problems linked to PMS.
- What could go wrong
- This is a small, early-stage study with only 40 participants. Results may not apply to everyone, and the exact benefits are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 30 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Gehad Mohamed Ali
Hurghada, Egypt
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