Influence of Beta Amyloid Imaging on Care of Patients Cognitive Complaints.

NCT ID: NCT02309723

Last Updated: 2017-04-10

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

315 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-09-30

Study Completion Date

2013-11-30

Brief Summary

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When older patients develop cognitive problems - like memory loss - there may be any of several underlying causes, sometimes occurring in combination. Clinicians have a better chance of providing appropriate treatment if they understand what the cause of the problem is. A diagnostic tool can help the patient by helping the clinician to make a more accurate diagnosis. This study investigates whether a new diagnostic tool - beta amyloid imaging - may potentially improve medical practice. The tool can potentially improve practice only if it can influence clinical judgment. This study investigates whether the provision of beta amyloid imaging information influences clinical judgment. The investigators will conduct a survey that presents clinicians with descriptions of hypothetical older patients with cognitive complaints. Some of the respondents also receive beta amyloid imaging information. The investigators will test the investigators hypothesis that the information will affect diagnostic judgment and management recommendations by comparing the responses of clinicians who receive the beta amyloid information to the responses of clinicians who do not.

Detailed Description

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Conditions

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Alzheimer's Disease Mild Cognitive Impairment

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Positive beta amyloid findings

Beta amyloid imaging results indicated a positive finding.

Group Type EXPERIMENTAL

Beta amyloid imaging

Intervention Type DEVICE

Negative beta amyloid findings

Beta amyloid imaging results indicated a negative finding.

Group Type EXPERIMENTAL

Beta amyloid imaging

Intervention Type DEVICE

No beta amyloid information

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Beta amyloid imaging

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Practicing clinicians describing their training and practice as any of the following: neurologist, geriatrician, psychiatrist.
* Included respondents must also attest that they are a physician who is experienced in the assessment and diagnosis of dementia.
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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GE Healthcare

INDUSTRY

Sponsor Role collaborator

Tufts Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Joshua T. Cohen, Ph.D

Role: STUDY_DIRECTOR

Tufts Medical Center

Peter J Neumann, ScD

Role: PRINCIPAL_INVESTIGATOR

Tufts Medical Center

Locations

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Tufts Medical Center

Boston, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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CEVR-2013-001

Identifier Type: -

Identifier Source: org_study_id

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