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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05126862
Other study ID # HSR 210113
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 10, 2021
Est. completion date April 2024

Study information

Verified date November 2023
Source University of Virginia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is conduct a pilot open trial of a web-based cognitive bias modification intervention to reduce anxiety symptoms in persons with Huntington's disease and persons with Parkinson's disease.


Description:

After being informed about the study and giving informed consent, participants will enroll in a pilot open trial of MindTrails, a web-based cognitive bias modification intervention. Participants will complete five, 20-minute MindTrails training sessions over five weeks. Additionally, assessments of anxiety, interpretation bias, and other related outcomes will be completed at baseline, week 3, week 5, and 2 months following the last training session. Participants will each complete a semi-structured interview to provide qualitative feedback about their experiences with MindTrails and anxiety.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 43
Est. completion date April 2024
Est. primary completion date July 9, 2023
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Diagnosis of Huntington's disease or Parkinson's disease - Age 21 or older - Has anxiety symptoms (NeuroQoL Anxiety short form >12) Exclusion Criteria: - Unable to read and understand English - Previously diagnosed with dementia - Not located in the USA

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
MindTrails
MindTrails is a web-based cognitive bias modification intervention. Training sessions are designed to encourage cognitive flexibility through repeated practice assigning benign resolutions to ambiguous, anxiety-provoking situations.

Locations

Country Name City State
United States University of Virginia Charlottesville Virginia

Sponsors (1)

Lead Sponsor Collaborator
University of Virginia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of participants completing at least 50% of the MindTrails sessions Proportion of participants completing at least 50% of the MindTrails sessions Between baseline and week 5
Primary Participant perceptions of perceived benefits and limitations of MindTrails Semi-structured interviews After completion of the intervention (week 5)
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