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Could empowering mothers be the key to better bedwetting care?

NCT ID NCT07753304

Symptom relief Sponsor: Cairo University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 07, 2026 · Last updated Aug 12, 2026 · Updated 2 times

Summary

This trial tests whether a structured, nurse-led empowerment program can boost mothers' knowledge and caregiving practices for children with nocturnal enuresis (bedwetting). Around 200 mothers of children aged 6-12 will either receive the program in small group sessions or continue with usual care. The study measures changes in mothers' knowledge, self-reported practices, and quality of life over three months. If successful, this approach could offer a practical, low-cost way to support families dealing with bedwetting.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A structured nurse-led behavioral empowerment program for mothers, delivered in small group sessions with an educational booklet.
What this could lead to
If effective, this program could become a simple, low-cost way to support mothers and improve caregiving for children with bedwetting, potentially easing family stress and improving outcomes.
What could go wrong
This is a single-center trial with a specific population, so results may not apply broadly. The program's success depends on mothers' engagement and may not directly change the child's bedwetting itself.

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

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

200 people

The number who actually took part.

Started

Sep 2024

Finished

Jun 2025

Lead sponsor

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

18 years and older

Sex

Female participants only

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria Mothers aged 18 years or older. Mothers of school-age children diagnosed with nocturnal enuresis. Child aged 6-12 years attending the outpatient urinary incontinence clinic at the Centre for Social and Preventive Medicine, Cairo University. Able to communicate in Arabic. Willing to participate and provide written informed consent. Available to complete baseline, post-intervention (4 weeks), and 3-month follow-up assessments. Exclusion Criteria Mothers of children with secondary nocturnal enuresis caused by serious neurological, endocrine, or structural urinary tract disorders. Mothers whose children have severe cognitive impairment or medical conditions preventing participation in the educational program. Mothers currently participating in another structured educational or behavioral intervention related to nocturnal enuresis. Mothers unwilling or unable to provide informed consent or complete study assessments. Mothers planning to relocate or unlikely to complete follow-up evaluations.

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Conditions

The condition(s) this trial relates to.

Empowerment nocturnal enuresis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Nocturnal enuresis Nocturnal enuresis in children

Contacts and locations

Locations

  • Faculty of nursing Cairo University

    Cairo, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.