RecruitingNot ApplicableNCT07213648
Modification of Threat Interpretation Bias to Reduce Anxiety in Neurodegenerative Movement Disorders (Aim 3)
Sponsor
University of Virginia
Enrollment
136 participants
Start Date
Nov 20, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to assess preliminary efficacy of a tailored cognitive bias modification for interpretation (CBM-I) app for reducing anxiety in Huntington's disease and Parkinson's disease.
Eligibility
Min Age: 21 Years
Inclusion Criteria2
- Clinical diagnosis of Huntington's disease or Parkinson's disease (genetic diagnosis of HD also acceptable)
- With anxiety symptoms (NeuroQoL Anxiety ≥12)
Exclusion Criteria6
- Cognitive decline precluding ability to consent or complete the intervention (MoCA 5 min/telephone ≤11)
- Unable to read and understand English
- Does not have regular access to an internet-connected device, capable of downloading and installing the mobile application (i.e., tablet or iPhone running iOS 10 or later or an Android phone running Android 5.0 or later)
- Not located in the USA
- \<21 years old
- Active suicidality based on the answer "yes" to questions 4, 5, or 6b of the Columbia-Suicide Severity Rating Scale (Screen version)
Interventions
BEHAVIORALMindTrails-Movement
CBM-I training app with active CBM-I training condition
OTHERWaitlist Control
Version of MindTrails-Movement app including surveys and list of support resources but without active CBM-I training component
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07213648
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