CONNECT4APOE: Telephone Versus Videoconference Communication for Remote Genetic Disclosure in the APOE4 Trial

Sponsor
University of Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT02978729
Collaborator
(none)
613
2
35.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Two-way videoconference remote genetic counseling
  • Other: Telephone remote genetic counseling
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
613 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
A Randomized Study of Telephone Versus Videoconference Communication for Remote Genetic Disclosure in the APOE4 Trial
Study Start Date :
Aug 1, 2016
Actual Primary Completion Date :
Jul 11, 2019
Actual Study Completion Date :
Jul 11, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Telephone

Telephone telegenetics counseling: A trained Penn genetic counselor will conduct genotype disclosure visits with the participant via telephone. The participant will be in a private room at the study site. Telephone sessions will utilize a private phone line. The genetic counselor will use standardized disclosure checklist and visual aids for the disclosure session.

Other: Telephone remote genetic counseling

Experimental: Videoconference

Two-way videoconferencing telegenetics counseling: A trained Penn genetic counselor will conduct genotype disclosure visits with the participant via two-way videoconferencing. The participant will be in a private room at the study site. Videoconferencing sessions will utilize tablets or laptops with web cameras and secure/confidential software for teleconferencing. The genetic counselor will use standardized disclosure checklist and visual aids for the disclosure session.

Other: Two-way videoconference remote genetic counseling

Outcome Measures

Primary Outcome Measures

  1. Satisfaction with genetic counseling services as measured by the Satisfaction with Genetic Services Scale [2-7 days]

  2. Satisfaction with genetic counseling services as measured by the Satisfaction with Remote Counseling Scale [2-7 days]

Secondary Outcome Measures

  1. Knowledge of Genetic Disease as measured by the Cancer Genetics Knowledge Scale [2-7 days, 6 weeks, 6 months, 12 months]

  2. Disease-specific distress as measured by the Impact of Events Scale [2-7 days, 6 weeks, 6 months, 12 months]

  3. 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]

  4. 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]

  5. Depression as measured by the GDS Short Form [2-7 days, 6 weeks, 6 months, 12 months]

  6. Anxiety as measured by the Mini State Trait Anxiety Inventory (mSTAI): [2-7 days, 6 weeks, 6 months, 12 months]

  7. Knowledge of Genetic Disease as measured by the ClinSeq Knowledge Scale [2-7 days, 6 weeks, 6 months, 12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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:

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Pennsylvania

Investigators

  • Principal Investigator: Angela R Bradbury, MD, University of Pennsylvania

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT02978729
Other Study ID Numbers:
  • 824225
First Posted:
Dec 1, 2016
Last Update Posted:
Nov 19, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by University of Pennsylvania
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 19, 2020