Expanded Protocol for Teleneurology Assessment Program for Creutzfeldt-Jakob Disease (TAPCJD)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Number of Participants who complete a Teleneurology Assessment
研究概览
简要总结
This observational study uses secure videoconference visits to follow people with Creuztzfeldt-Jakob disease (CJD) over time. The study collects information about participants' symptoms, neurological function, thinking and memory, and ability to perform daily activities. It also collects information from study partners about the participant and about their own well-being and experiences as caregivers. The goal of the study is to better understand how CJD changes over time and to evaluate the use of remote assessments for CJD research and surveillance.
详细描述
TAPCJD is a longitudinal observational study designed to collect standardized clinical information from individuals with Prion Disease using remote videoconference assessments. The study builds upon an earlier TAPCJD pilot study and is intended to improve understanding of the clinical course of Prion Disease and the use of remote assessments in prion disease research and surveillance.
Participants take part in videoconference visits with a study partner who knows them well. Assessments include clinical history, cognitive assessment, modified neurological examination, functional assessment, and evaluation of neuropsychiatric symptoms. Study partners also complete measures related to caregiver well-being and burden.
Videoconference evaluations occur at baseline and at approximately 1, 2, 4, and 6 months, followed by evaluations every three months for the duration of the participant's survival. Assessments may be modified or omitted depending on the participant's clinical condition. Participation ends at death, if the clinical diagnosis changes and no longer includes prion disease, or if the participant or study partner chooses to discontinue participation.
The study also examines the reliability and validity of standardized remote assessments, caregiver burden and well-being, and the potential benefits of caregiver support-group participation.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Study Participant Inclusion Criteria:
- •Age greater than 18 years.
- •Participant must have a study partner who will be present with the participant for all videoconference evaluations (in the same physical location).
- •Participant meets criteria for definite or probable prion disease or is a known PRNP mutation carrier with active disease.
- •Participant and/or appropriate proxy consents to study participation.
- •Study Partner Inclusion Criteria:
- •Age greater than 18 years.
- •Study partner must be present with the participant for all videoconference evaluations and must have knowledge of the participant's abilities before the onset of illness. The study partner should be with the participant at least three times per week or for a total of five hours per week as the illness progresses.
- •Study partner must have internet access and a computer, smartphone, or tablet with videoconference capabilities.
- •Study partner consents to study participation.
排除标准
- •Study Participant Exclusion Criteria:
- •Participant's diagnosis is most likely not prion disease.
- •Participant or study partner is less than 18 years of age.
- •Participant or study partner does not have internet access or a computer, smartphone, or tablet with videoconference capabilities.
- •Participant does not have a study partner.
- •Study Partner Exclusion Criteria:
- •Study partner is less than 18 years of age.
- •Study partner does not have sufficient knowledge of the participant's abilities prior to the onset of illness or does not have sufficient ongoing contact with the participant.
- •Study partner does not have internet access or a computer, smartphone, or tablet with videoconference capabilities.
- •Study partner does not consent to study participation.
研究组 & 干预措施
Prion Disease
Adults with definite or probable prion disease, or known PRNP mutation carriers with active disease, who participate in longitudinal videoconference assessments with a study partner.
干预措施: Teleneurology Assessment (Other)
结局指标
主要结局
Number of Participants who complete a Teleneurology Assessment
时间窗: Baseline through end of participant follow-up, up to 10 years.
The number of participants who complete at least on standardized teleneurology assessment by videoconference will be recorded
次要结局
未报告次要终点
研究者
Brian Appleby
Physician
University Hospitals Cleveland Medical Center