Not Yet RecruitingNot Applicable

Aerobic Versus Resistance Exercises on Disability After Abdominal Myomectomy

60 participantsStarted 2026-06-25

Plain-language summary

This study will be conducted to compare aerobic and resistance exercises on disability after abdominal myomectomy.

Who can participate

Age range

30 Years – 60 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: * All patients are conscious and ambulant. * Their ages ranged from 30-60 years old. * All patients will be under post abdominal myomectomy (6-12 months) management program. * All patients will not suffer from any complication post abdominal myomectomy, except weakness of abdominal muscles. * All patients will receive and agreed to sign the informed consent form. Exclusion Criteria: * The patient who has cardiovascular diseases, or uncontrolled hypertension. * The patient who has cardiac pacemakers or other implanted electronic devices. * Uncooperative patients. * Patients who have cardiopulmonary diseases. * Patients who have psychic disorders. * Patients with neuromuscular diseases. * Pregnant female. * Patients who have any endocrine, metabolic, renal or hepatic diseases. Patients who have an open wound at or near the treatment site.

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

functional disability

Timeframe: up to 12 weeks

pain intensity

Timeframe: up to 12 weeks

Trial details

NCT IDNCT07661147

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-10-30

Contact for this trial

norhan khalaf, master

01018426731 Khalafnourhan.nk@gmail.com

View on ClinicalTrials.gov More Myomectomy trials