MS and motherhood: what shapes Women's choices?

NCT ID NCT07829822

NEW Knowledge-focused Sponsor: Assiut University Source: ClinicalTrials.gov ↗

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Recruiting now
This trial is taking on new participants right now.
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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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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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

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Status unknown
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First seen Sep 21, 2026 · Last updated Sep 21, 2026

Summary

Women with multiple sclerosis face complex decisions about marriage, pregnancy, and motherhood. This study explores how women of reproductive age in Assiut Governorate, Egypt, make these choices. Researchers will survey married women using questionnaires and interview both married and single women to understand their concerns, fertility intentions, and the factors that influence their decisions. The goal is to identify gaps in reproductive health counseling and support for women with MS.

What this could mean

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

What this could lead to
If successful, this study could identify gaps in reproductive health counseling for women with multiple sclerosis and help shape services that better address their concerns about pregnancy, motherhood, and family planning.
What could go wrong
This is an observational study, so it cannot prove cause and effect. The findings may not apply to women with multiple sclerosis in other regions or countries, and the results depend on what participants choose to share in interviews and questionnaires.

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.

Participants

About 272 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2027

An estimate. Start dates often move.

Expected to finish

Oct 2031

An estimate. End dates often move.

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.

Who is studied

The quantitative study population will include married women aged 18-49 with confirmed multiple sclerosis who attend the selected study sites during the study period. On the other hand, the qualitative population will include single, currently married, divorced and widowed/ever-married women aged 18-49 years with confirmed MS, as appropriate to the study sites and the qualitative sampling plan.

Ages

18 to 49 years

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.

o Inclusion criteria Women who are: * Within reproductive age group (18-49 years). * With confirmed diagnosis of multiple sclerosis according to the 2024 Revised McDonald Criteria (31). * Able to communicate, agree to participate in the study and provide informed consent. * Exclusion Criteria Women with: * Severe cognitive impairment or psychiatric illness affects their ability to participate in the study. * Acute medical or neurological deterioration at the time of recruitment makes participation inappropriate or burdensome. * Any condition judged by the clinical team or research team to make participation unsafe or to compromise the validity of the interview.

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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

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  1. The official record

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