Study explores the hidden toll of rare genetic diseases on families

NCT ID NCT07348926

First seen Jun 27, 2026 · Last updated Jun 27, 2026

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for FUNCTIONAL IMPAIRMENT are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

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.

Contacts and locations

Locations

  • Bahcesehir University

    RECRUITING

    Istanbul, 34053, Turkey (Türkiye)

More trials for these conditions

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