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RECRUITINGINTERVENTIONAL

Modification of Threat Interpretation Bias to Reduce Anxiety in Neurodegenerative Movement Disorders (Aim 3)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - Clinical diagnosis of Huntington's disease or Parkinson's disease (genetic diagnosis of HD also acceptable) - With anxiety symptoms (NeuroQoL Anxiety ≥12) Who Should NOT Join This Trial: - 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) Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Clinical diagnosis of Huntington's disease or Parkinson's disease (genetic diagnosis of HD also acceptable) * With anxiety symptoms (NeuroQoL Anxiety ≥12) Exclusion Criteria: * 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)

Treatments Being Tested

BEHAVIORAL

MindTrails-Movement

CBM-I training app with active CBM-I training condition

OTHER

Waitlist Control

Version of MindTrails-Movement app including surveys and list of support resources but without active CBM-I training component

Locations (1)

Univeristy of Virginia School of Nursing
Charlottesville, Virginia, United States