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Study explores the hidden toll of rare genetic diseases on families

NCT ID NCT07348926

First seen Jan 28, 2026 · Last updated Jun 18, 2026 · Updated 22 times

Summary

This study looks at how the daily abilities of young children (0-4 years) with rare genetic disorders impact their families' mental health and quality of life. Researchers will assess the child's functional independence and measure parents' depression and well-being through questionnaires. The goal is to help healthcare providers offer better support, such as physiotherapy and counseling, tailored to each family's needs.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Bahcesehir University

    RECRUITING

    Istanbul, 34053, Turkey (Türkiye)

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

Conditions

The condition(s) this trial relates to.

Depression hereditary disease

As listed by the trial registrant

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