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The Study of the Impact of Disclosing Imaging Study Information to Trial Participants

I

Institute for Neurodegenerative Disorders

Status

Completed

Conditions

Parkinsonian Syndrome
Parkinson

Treatments

Behavioral: A series of questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT00354003
IMAG-DIS 01

Details and patient eligibility

About

The overall goal of the study is to evaluate how research participants in Parkinson Disease studies that include brain imaging with a dopamine transporter ligand choose to receive the imaging data and what is the impact of the imaging data information on the management of their symptoms.

Full description

Research participants who previously underwent ß-CIT imaging will be contacted by the staff at IND to enquire whether they would like to receive their ß-CIT scan data. After signing a Research Participant Information and Consent Form, all research participants will be asked to complete a questionnaire prior to receipt of their imaging data. Those research participants requesting imaging data will be sent their data by IND and may review their data with IND (by phone) and/ or with their study investigator. All research participants will be asked to respond to a second questionnaire after receiving their imaging data and to a third study questionnaire approximately six weeks following receipt of their imaging data.

Enrollment

800 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Previous participation in imaging study as described within the protocol

Exclusion criteria

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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