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NCT02881931 · ClinicalTrials.gov registry record
FuRST 2.0 Cognitive Pre-Testing
A clinical trial of Huntington's Disease, sponsored by CHDI Foundation.
- Completed
- Registry status
- 75
- Enrollment target
- 4
- Study locations
NCT02881931 is a study of Huntington's Disease that has completed, run by CHDI Foundation. The registered enrollment target is 75 participants, below the 4,784-participant average among 8 other Huntington's Disease trials with a reported enrollment target (98% lower). The trial reports 4 study locations across 4 states.
The verdict
NCT02881931, a study of Huntington's Disease, has completed, sponsored by CHDI Foundation.
- COMPLETED
- Registry status
- 75 participants
- Enrollment target
- 4
- Study locations
Study Summary
The FuRST 2.0 scale is being developed as a Patient Reported Outcome (PRO) with information coming directly from the Huntington's Disease Gene Expansion Carrier (HDGEC) and companion through self-report. The purpose of this study is to identify real or potential comprehension or usage problems with questionnaire items or response options. Through a process of structured cognitive de-briefing with HDGEC participants and companions, independently, followed by qualitative analysis, the final phrasing of the individual items and response options for the scale will be generated. Depending on the results of the first round of cognitive pre-testing, additional rounds of cognitive pre-testing may be required.
Conditions Studied
Interventions
- BEHAVIORAL FuRST 2.0
Study Locations (4)
Colorado
- Rocky Mountain Movement Disorders Center, P.C. - Englewood
Kansas
- Hereditary Neurology Disease Centre, Inc. - Wichita
New York
- Columbia University - New York
Ontario
- CENTRE FOR MOVEMENT DISORDERS (Neuropharm Consulting) - Toronto
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2017-02-28 |
| Est. Completion | 2017-07-28 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02881931
The ClinicalTrials.gov registry entry for NCT02881931 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,784-participant average among 8 other Huntington's Disease trials with a reported enrollment target (98% lower). The listed sponsor is CHDI Foundation, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Huntington's Disease appearing as the primary indexed condition, and to 1 intervention - of which FuRST 2.0 is the first listed.
NCT02881931 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Colorado, Kansas, New York.
Frequently Asked Questions
What is clinical trial NCT02881931 about?
NCT02881931 is a clinical study titled "FuRST 2.0 Cognitive Pre-Testing". The FuRST 2.0 scale is being developed as a Patient Reported Outcome (PRO) with information coming directly from the Huntington's Disease Gene Expansion Carrier (HDGEC) and companion through self-report. The purpose of this study is to identify real or potential comprehension or usage problems with ...
What is the current status of trial NCT02881931?
This trial is currently completed. The enrollment target is 75 participants. The study started on 2017-02-28. Estimated completion is 2017-07-28.
What conditions does trial NCT02881931 study?
This clinical trial studies the following conditions: Huntington's Disease.
What interventions are being tested in trial NCT02881931?
The interventions under investigation include: FuRST 2.0 (BEHAVIORAL).
Who is sponsoring clinical trial NCT02881931?
This trial is sponsored by CHDI Foundation, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02881931 being conducted?
This trial has 4 study locations across Colorado, Kansas, New York, Ontario. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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