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Enhancing Consent for Alzheimer's Research (BWP-AD)

Primary Purpose

Alzheimer Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Enhanced Consent Procedure
Routine Consent Procedure
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Alzheimer Disease focused on measuring computer assisted instruction, decision making, educational resource design /development, executive function

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Clinical diagnosis of mild to moderate possible or probable AD or demographically comparable healthy comparison subjects
  • Fluency in English
  • 50 yrs and older
  • Informed written consent (or written assent with consent from legally authorized representative)

Exclusion Criteria:

  • Diagnosis of Lewy Body Dementia or Mild Cognitive Impairment
  • MMSE less than 15
  • Physical or medical conditions that preclude participants from completing tasks
  • Healthy comparison volunteers if they have a known neurologic or psychiatric condition that could impair neurocognitive functioning

Sites / Locations

  • Veterans Affairs San Diego Healthcare System

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Active Comparator

Active Comparator

Arm Label

Enhanced consent - A

Enhanced consent - B

Routine consent - A

Routine consent - B

Arm Description

The intervention was an enhanced consent process, including a multimedia aid for a moderate risk hypothetical protocol

The intervention was an enhanced consent process, including multimedia aide for a higher risk hypothetical protocol

This was a comparison condition - a routine consent process, including a printed consent document, for a moderate risk hypothetical protocol

This was a comparison condition - a routine consent process, including a printed consent document, for a higher risk hypothetical protocol

Outcomes

Primary Outcome Measures

Level of Understanding
Modified version of the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR) Understanding subscale. Minimum value = 0, Maximum value = 26; higher scores represent better performance
Appreciation
MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR) Appreciation subscale Minimum score = 0, Maximum Score = 6; Higher scores represent better understanding
Reasoning
Reasoning subscale of the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR) Minimum score = 0; Maximum Score = 8; Higher scores mean better reasoning capacity
Expression of a Choice
Expression of a Choice subscale of the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR); Minimum score = 0, Maximum score = 2; higher scores represent more intact ability to express a clear choice

Secondary Outcome Measures

Level of Satisfaction With Consent Process
Question - "The consent process was" rated from "Very easy" to "Very Hard" Very Easy Easy No effect Hard Very hard Higher scores mean more difficult (less satisfaction) with the consent process with 1 being "Very Easy" and 5 being "Very hard"
Expressed Willingness to Participate in the Hypothetical Protocol
Question about willingness to consent in the protocol described 0 = No = Yes = Unsure

Full Information

First Posted
March 28, 2007
Last Updated
June 2, 2023
Sponsor
University of California, San Diego
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT00453544
Brief Title
Enhancing Consent for Alzheimer's Research
Acronym
BWP-AD
Official Title
Enhancing Consent for Alzheimer's Research
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
April 2006 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
National Institute on Aging (NIA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the efficacy of an enhanced consent procedure for patients with mild-to-moderate Alzheimer disease, and to identify factors and patient characteristics that predict the degree to which enhanced consent is more beneficial than routine consent procedures.
Detailed Description
Alzheimer disease can impair the capacity of patients to give informed consent for research participation. Studies of informed consent involving other patient populations suggest better understanding of consent-relevant information may be achieved through modifications in the consent delivery process, including incorporation of multimedia learning tools into the consent discussion. In the present study, participants with Alzheimer disease and age-comparable healthy participants will be randomly assigned to review a hypothetical research protocol via routine or enhanced consent procedures. Participants will also complete standard cognitive and other rating scales so that we can characterize the sample, as well as evaluate the degree to which specific characteristics may be associated with need for enhanced consent procedures. Advances in the methods to optimize the informed consent process should enable future research participants to make more fully informed decisions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease
Keywords
computer assisted instruction, decision making, educational resource design /development, executive function

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
252 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enhanced consent - A
Arm Type
Experimental
Arm Description
The intervention was an enhanced consent process, including a multimedia aid for a moderate risk hypothetical protocol
Arm Title
Enhanced consent - B
Arm Type
Experimental
Arm Description
The intervention was an enhanced consent process, including multimedia aide for a higher risk hypothetical protocol
Arm Title
Routine consent - A
Arm Type
Active Comparator
Arm Description
This was a comparison condition - a routine consent process, including a printed consent document, for a moderate risk hypothetical protocol
Arm Title
Routine consent - B
Arm Type
Active Comparator
Arm Description
This was a comparison condition - a routine consent process, including a printed consent document, for a higher risk hypothetical protocol
Intervention Type
Other
Intervention Name(s)
Enhanced Consent Procedure
Intervention Description
This is a procedure involving use of multimedia materials, as well as standard review with research staff, to see if the research consent procedure can be improved
Intervention Type
Other
Intervention Name(s)
Routine Consent Procedure
Intervention Description
This is a procedure designed to be in accord with standard research consent practices (and lacks multimedia aids)
Primary Outcome Measure Information:
Title
Level of Understanding
Description
Modified version of the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR) Understanding subscale. Minimum value = 0, Maximum value = 26; higher scores represent better performance
Time Frame
Within session - administered approximately 2-3 minutes after completion of the simulated consent process.
Title
Appreciation
Description
MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR) Appreciation subscale Minimum score = 0, Maximum Score = 6; Higher scores represent better understanding
Time Frame
Within session - immediately following administration of the MacCAT-CR Understanding subscale
Title
Reasoning
Description
Reasoning subscale of the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR) Minimum score = 0; Maximum Score = 8; Higher scores mean better reasoning capacity
Time Frame
Within session-immediately following administration of the MacCAT-CR Appreciation subscale
Title
Expression of a Choice
Description
Expression of a Choice subscale of the MacArthur Competence Assessment Tool for Clinical Research (MacCAT-CR); Minimum score = 0, Maximum score = 2; higher scores represent more intact ability to express a clear choice
Time Frame
Within session--immediately following administration of the MacCAT-CR Reasoning subscale
Secondary Outcome Measure Information:
Title
Level of Satisfaction With Consent Process
Description
Question - "The consent process was" rated from "Very easy" to "Very Hard" Very Easy Easy No effect Hard Very hard Higher scores mean more difficult (less satisfaction) with the consent process with 1 being "Very Easy" and 5 being "Very hard"
Time Frame
Within session
Title
Expressed Willingness to Participate in the Hypothetical Protocol
Description
Question about willingness to consent in the protocol described 0 = No = Yes = Unsure
Time Frame
Within session-last item of the Expression of a Choice Subscale, which itself was measured immediately after the MacCAT-CR Reasoning subscale

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of mild to moderate possible or probable AD or demographically comparable healthy comparison subjects Fluency in English 50 yrs and older Informed written consent (or written assent with consent from legally authorized representative) Exclusion Criteria: Diagnosis of Lewy Body Dementia or Mild Cognitive Impairment MMSE less than 15 Physical or medical conditions that preclude participants from completing tasks Healthy comparison volunteers if they have a known neurologic or psychiatric condition that could impair neurocognitive functioning
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barton W. Palmer, PhD
Organizational Affiliation
UCSD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Veterans Affairs San Diego Healthcare System
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11329391
Citation
Kim SY, Caine ED, Currier GW, Leibovici A, Ryan JM. Assessing the competence of persons with Alzheimer's disease in providing informed consent for participation in research. Am J Psychiatry. 2001 May;158(5):712-7. doi: 10.1176/appi.ajp.158.5.712.
Results Reference
background
PubMed Identifier
15494623
Citation
Alzheimer's Association. Research consent for cognitively impaired adults: recommendations for institutional review boards and investigators. Alzheimer Dis Assoc Disord. 2004 Jul-Sep;18(3):171-5. doi: 10.1097/01.wad.0000137520.23370.56.
Results Reference
background
PubMed Identifier
7053558
Citation
Kolata G. Alzheimer's research poses dilemma. Science. 1982 Jan 1;215(4528):47-8. doi: 10.1126/science.7053558.
Results Reference
background
PubMed Identifier
11331139
Citation
Dunn LB, Jeste DV. Enhancing informed consent for research and treatment. Neuropsychopharmacology. 2001 Jun;24(6):595-607. doi: 10.1016/S0893-133X(00)00218-9.
Results Reference
background
PubMed Identifier
28154452
Citation
Palmer BW, Harmell AL, Pinto LL, Dunn LB, Kim SY, Golshan S, Jeste DV. Determinants of Capacity to Consent to Research on Alzheimer's disease. Clin Gerontol. 2017;40(1):24-34. doi: 10.1080/07317115.2016.1197352. Epub 2016 Jun 7.
Results Reference
result
PubMed Identifier
29182458
Citation
Palmer BW, Harmell AL, Dunn LB, Kim SY, Pinto LL, Golshan S, Jeste DV. Multimedia Aided Consent for Alzheimer's Disease Research. Clin Gerontol. 2018 Jan-Feb;41(1):20-32. doi: 10.1080/07317115.2017.1373177. Epub 2017 Nov 28.
Results Reference
result

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Enhancing Consent for Alzheimer's Research

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