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N/A N=370 Randomized Other

GEnetic Counseling Through Virtual Visits in Parkinson's Disease

Parkinson Disease

Enrolled (actual)
370
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: Genetics Knowledge — 16; 17; 17; 16 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
IMAGINE-PD (Other); Virtual genetic counseling (Other); Telephone genetic counseling (Other)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
University of Pennsylvania
Primary completion
Oct 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Genetics Knowledge
16; 17; 17; 16
PRIMARY
Genetic Counseling Satisfaction (Post-Test)
24; 25; 25; 26
PRIMARY
Test-Related Distress
0; 0; 0; 0
SECONDARY
Genetic Counseling Satisfaction (Pre-Test)
22; 23; 24; 25
SECONDARY
Depression
3; 3; 3; 3
SECONDARY
Depression
3; 3; 3; 3
SECONDARY
State-Trait Anxiety Index-State Score
35; 36; 35; 36
SECONDARY
State-Trait Anxiety Index -State Score
35; 36; 34.5; 36
SECONDARY
State-Trait Anxiety Index -Trait Score
34; 34; 35; 35
SECONDARY
State-Trait Anxiety Index -Trait Score
34; 34; 35; 35
SECONDARY
Quality of Life in Parkinson's Disease
20.99; 15.31; 17.79; 19.22
SECONDARY
Quality of Life in Parkinson's Disease
20.99; 15.31; 17.79; 19.22
SECONDARY
Test-Related Distress
0; 0; 0; 0

Summary

The research study is being conducted to compare methods of virtual genetic counseling for people with Parkinson's disease.

Eligibility Criteria

Inclusion Criteria

  • Provision of signed and dated informed consent form
  • Stated willingness to have clinical confirmation genetic testing, and comply with all study procedures and availability for the duration of the study
  • Male or female, over the age of 21.
  • English Speaking

Exclusion Criteria

  • Prior genetic counseling and/or clinical testing specifically for Parkinson's disease
  • Montreal Cognitive Assessment (MoCA) < 21, or a prior diagnosis of dementia during the screening phase
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04527146). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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