CompletedNot Applicable

Milk Production and Body Weight Response to Suggested Protocol in Obese Lactating Women

Egypt72 participantsStarted 2025-05-20

Plain-language summary

This study will investigate the milk production and body weight response of both mother and the newborn to aerobic exercise in obese lactating women.

Who can participate

Age range

25 Years – 35 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: * Multiparous obese mothers having number of parity ranges from two to four times. * Lactating mothers within 2nd month after delivery. * All of them diagnosed by gynecologist as having insufficient lactation * Age will range from 25-35 years old. * Body mass index: 30-40 Kg/m². Exclusion Criteria: * Lactating women suffering from postpartum hemorrhage * Poor mammary development * Cardio respiratory disease * Diabetes mellitus * Breast cancer * Getting pregnant again during breast feeding period * Mental disorders * Previous surgeries in the chest, breast or the surrounding area * Anemia * Having twins or causes that hindering normal breast feeding as (mastitis, retracted, cracked, inflamed or inverted nipple)

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

Assessment of the degree of improvement in the flow of milk

Timeframe: 6 weeks

Serum prolactin level

Timeframe: 6 weeks

Weight of the baby

Timeframe: 6 weeks

Weight of the mother

Timeframe: 6 weeks

Trial details

NCT IDNCT06975527

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-08-30

View on ClinicalTrials.gov More Breastfeeding trials

Who can participate

Age range

25 Years – 35 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.