Rare Genetic Disorders

2

Review clinical trials related to Rare Genetic Disorders. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Using a Speech-Generating Device to Support Communication in Rare Genetic Conditions

Individuals with rare genetic conditions may experience a delay or loss of developmental skills. Many have limited verbal speech. The aim of this clinical trial is to examine how well a speech-generating device supports the communication skills of participants with a rare genetic condition. The speech-generating device is a communication program loaded onto an iPad. This is a crossover trial, meaning that each participant will receive both the treatment (device) and a control (usual care; no device) phase. The order in which each participant receives the device versus the usual care (no device) will depend on which group the participant is assigned to. The changes in communication in each phase will then be compared. During the trial, participants can expect to complete a series of assessments and attend a total of 2 x 1-hour therapy session per week for 6 weeks.

Participants needed: 38
Trial details
Age: 3-12Biological sex: AllType: InterventionalSponsor: Murdoch Childrens Research InstituteUpdated: May 26, 2026Locations: 1
Eligibility criteria

Is between the ages of 3 and 12 years, inclusive, at the time of enrolment [+5]

Has an additional or dual genetic variation (as this is likely to cause multiple... [+4]

Status: Recruiting

The Relationship Between Functional Independence and Family Well-being in Children With Rare Genetic Disorders

This study aims to examine the psychological status and quality of life of families with children who have rare genetic disorders. The focus of the study is to understand how the child's level of functional independence relates to the well-being of the family. Functional independence will be assessed using standardized tools, and parental psychological status and quality of life will be evaluated with validated questionnaires. The information gathered from this study may help improve the understanding of how rare genetic disorders affect family dynamics and daily functioning. The results may guide health care professionals in planning family-centered physiotherapy, psychological support, and care programs.

Participants needed: 45
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Bahçeşehir UniversityUpdated: Jan 16, 2026Locations: 1
Eligibility criteria

Caregivers of children aged 0-4 years diagnosed with a rare genetic disorder. [+3]

Caregivers who have cognitive or language limitations that prevent them from com... [+2]