The Rett Syndrome Global Registry
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 5,000
- 试验地点
- 1
- 主要终点
- Frequency of genetic mutation types and clinical diagnoses.
研究概览
简要总结
The Rett Global Registry is a fully remote, global, caregiver-reported registry to collect information about caring for a loved one with Rett syndrome. In addition, caregivers have the ability to track and graph their loved one's symptoms and care strategies over time, store information for central access, and opt-in to complete medical record consolidation and summary. Qualified researchers and therapeutic developers may request access to de-identified aggregate information to further Rett research, or assist with clinical development planning to facilitate and expedite more effective clinical trials.
详细描述
The Rett Syndrome Global Registry is a fully remote, global, caregiver-reported registry intended to meet the needs of caregivers, clinicians and researchers, and therapeutic developers with the goal to increase our understanding of this rare disorder, support better outcomes for those with Rett syndrome, and facilitate improved therapeutic development. The Rett Global Registry allows families to provide data about their experience with Rett syndrome to improve their loved one's care while contributing to research. Participants may opt in to track and graph symptoms and care strategies over time to support day-to-day care. Participants may also access aggregate data to see similarities and differences in care strategies and consolidate their personal information in a central location. Participants may opt-in to complete medical record consolidation and summary that is centrally accessible, able to be shared with care providers, and utilized for research.
The registry database is designed and maintained to clinical trial standards and supports research and therapeutic development while meeting or exceeding federal privacy and confidentiality requirements. These datasets including caregiver-reported Rett syndrome progression, quality of life, at home day-to-day data, and consolidated medical records from office visits or hospital stays, provides unique and previously unused sources of information important for improving our understanding of Rett syndrome, allow additional avenues of research, and support therapeutic development. Specifically, the registry is intended to assist with clinical development planning, trial design, trial endpoints, and regulatory filings.
研究设计
- 研究类型
- Observational
- 观察模型
- Family Based
- 时间视角
- Cross Sectional
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Parent/caregiver must be willing and able to provide written informed consent electronically prior to entering data into the registry.
- •Rett individuals of any age, living or deceased, must have a diagnosis of Rett syndrome and/or have a mutation in MECP2.
排除标准
- •Individuals who have a genetic mutation that is inconsistent with Rett syndrome or who have a different disorder.
- •Individuals with MECP2 Duplication Syndrome
结局指标
主要结局
Frequency of genetic mutation types and clinical diagnoses.
时间窗: 1 year
Measured by data obtained from genetic reports and caregiver-reported clinical diagnoses of enrolled patients.
Caregiver report of the composition and frequency of medication and over-the-counter treatments over time.
时间窗: 5 years
Measured by the percent of individuals receiving these care strategies by symptom between 1 and 4 times per year.
Caregiver report of developmental milestone achievement over time.
时间窗: 5 years
Measured by the percent of individuals who have achieved developmental milestones between 1 and 4 times per year.
Caregiver report of composition and frequency of co-morbidities over time.
时间窗: 5 years
Measured by the type and number of non-Rett medical conditions between 1 and 4 times per year.
Caregiver report of symptom burden and development history over time.
时间窗: 5 years
Measured by the percent of individuals who report symptoms and their intervention requirements between 1 and 4 times per year.
Caregiver report of the composition and frequency of physician specialty utilization and care received at Rett Clinics over time.
时间窗: 5 years
Measured by the type and number of physician specialties used to manage symptoms and the number of individuals who receive care at a Rett clinic between 1 and 2 times per year.
Caregiver report of the composition of the barriers to clinical trial participation over time.
时间窗: 5 years
Measured by the type and number of reasons given for individuals not able or willing to participate in clinical trials between 1 and 2 times per year.
次要结局
- Caregiver report of the frequencies of the level of effectiveness, degree of side effect severity, and other symptom impacts of medications and over-the-counter treatments over time.(5 years)
- Percent of individuals using registry features, including tracking, medical record consolidation, central storage, and family connections over time.(5 years)
- Caregiver report of the frequencies of the level of effectiveness for therapies, diets and equipment use over time.(5 years)
- Caregiver report of the percent of individuals requiring emergency care and unplanned hospital admissions over time.(5 years)