NCT07684495

Brief 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.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Jul 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress33%
Jul 2026Sep 2026

First Submitted

Initial submission to the registry

June 29, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

July 3, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 20, 2026

Expected
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Last Updated

July 6, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

June 29, 2026

Last Update Submit

June 29, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Memory function

    Assessment of memory function will be done by the free recall test. The word list will contain 10 words selected randomly. These words would be administered to the patient one by one with interval time 1 second between each word with total words presentation time 10 seconds. The presentation of these words will be though a digital screen using a designed video showing these words arranged in order with a fixed interval 1 second between each word. The patient will be instructed immediately to recall these words verbally at any order. The total score is 10 and one point will be accounted for each word will be recalled correctly

    6 weeks

  • Prospective and retrospective memory questionnaire (PRMQ)

    It will be used to assess memory functions. The measure consists of 16 individual items. The Structure of the PRMQ consists of 16 Items total , each item is rated on a 5-point scale (1 = Never , 2 = Rarely , 3 = Sometimes , 4 = Often , 5 = Very Often). These 16 items, evenly divided into 8 prospective memory items and 8 retrospective memory items. Each item describes a common memory lapse, giving a high score to an item means a high memory deficits at that item. The total score ranges from 16 to 80, with higher scores indicating a greater frequency of memory lapse and deficit.

    6 weeks

Secondary Outcomes (2)

  • Perceived Stress Scale (PSS)

    6 weeks

  • Cervical pain intensity

    6 weeks

Study Arms (2)

Aerobic exercise group

EXPERIMENTAL

The participants will receive aerobic exercise program for 30 minutes, 3 sessions per week for 6 weeks.

Other: Aerobic exercise

Sub occipital myofascial release group

EXPERIMENTAL

The participants will receive sub occipital myofascial release treatment 3 sessions per week for 6weeks.

Other: Sub occipital myofascial release

Interventions

A moderate-intensity aerobic exercise session on a treadmill consists of three phases: warm-up, active phase, and cool-down. The warm-up lasts 5-10 minutes and involves walking at minimum speed (2.0 - 3.0 km/h) with a slight incline (1 -2%) or as tolerated. The active phase, lasting 20-30 minutes, maintains a brisk walking or light jogging pace with moderate speed (4.5-6.5 km/h) or as tolerated. This phase can include steady-state jogging or intervals of walking and jogging to sustain cardiovascular engagement. Finally, the cool-down phase lasts 5-10 minutes, where the speed is gradually reduced to 2.0 - 3.0 km/h, allowing the heart rate to decrease safely.

Aerobic exercise group

The patient will be asked to take a supine position, and a pillow will be placed under the patient's head for comfort until starting the procedure, the patient will be instructed to be relaxed, then the therapist will sit at the head of the bed and will place both hands underneath the patient's head in the occipital region. The therapist should then feel for the occipital ridge along the scalp and move the hands slightly caudal until the muscle is felt. The therapist then will flex the fingers upward against the suboccipital muscles and this position will be hold for 3 to 5 minutes or until significant muscle tension will be released.

Sub occipital myofascial release group

Eligibility Criteria

Age18 Years - 30 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gehad Mohamed Ali

Hurghada, Egypt

Location

MeSH Terms

Conditions

Premenstrual Syndrome

Interventions

Exercise

Condition Hierarchy (Ancestors)

Menstruation DisturbancesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Elham Hassan, As Professor

    Cairo University

    STUDY DIRECTOR
  • Amel Youssef, Professor

    Cairo University

    STUDY CHAIR

Central Study Contacts

Gehad Ali, Bachelor

CONTACT

Asmaa Mohammed, PHD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

June 29, 2026

First Posted

July 6, 2026

Study Start

July 3, 2026

Primary Completion (Estimated)

September 20, 2026

Study Completion (Estimated)

September 30, 2026

Last Updated

July 6, 2026

Record last verified: 2026-06

Locations