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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02978729
Other study ID # 824225
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2016
Est. completion date July 11, 2019

Study information

Verified date November 2020
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare two methods for remote genetic counseling (telephone and two-way videoconferencing) for patients who are receiving disclosure of their APOE (apolipoprotein E) genotype. The target population will consist of males and females in the age range of 60-75 years who, as potential participants in a study (Generation Study), will need to receive genetic counseling and disclosure of APOE genotype. Subjects must be willing to receive genetic counseling and disclosure remotely. Subjects must be willing to be randomized to either telephone arm or videoconference arm.


Recruitment information / eligibility

Status Completed
Enrollment 613
Est. completion date July 11, 2019
Est. primary completion date July 11, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 75 Years
Eligibility Inclusion Criteria: 1. Eligible to participate in the Generation Study 2. Ability to provide consent 3. Ability to communicate and hear in English Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Two-way videoconference remote genetic counseling

Telephone remote genetic counseling


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Pennsylvania

Outcome

Type Measure Description Time frame Safety issue
Primary Satisfaction with genetic counseling services as measured by the Satisfaction with Genetic Services Scale 2-7 days
Primary Satisfaction with genetic counseling services as measured by the Satisfaction with Remote Counseling Scale 2-7 days
Secondary Knowledge of Genetic Disease as measured by the Cancer Genetics Knowledge Scale 2-7 days, 6 weeks, 6 months, 12 months
Secondary Disease-specific distress as measured by the Impact of Events Scale 2-7 days, 6 weeks, 6 months, 12 months
Secondary Perceived risk of Alzheimers Disease as measured by questionnaire items measuring perceived risk in quantitative, qualitative, and relative terms 2-7 days, 6 weeks, 6 months, 12 months
Secondary Responses to Genetic Testing as measured by the Impact of Genetic Testing for Alzheimer's disease (IGT-AD) scale 2-7 days, 6 weeks, 6 months, 12 months
Secondary Depression as measured by the GDS Short Form 2-7 days, 6 weeks, 6 months, 12 months
Secondary Anxiety as measured by the Mini State Trait Anxiety Inventory (mSTAI): 2-7 days, 6 weeks, 6 months, 12 months
Secondary Knowledge of Genetic Disease as measured by the ClinSeq Knowledge Scale 2-7 days, 6 weeks, 6 months, 12 months
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