Ignite Creation Date:
2025-12-26 @ 10:46 PM
Ignite Modification Date:
2025-12-26 @ 10:46 PM
Study NCT ID:
NCT00105612
Status:
COMPLETED
Last Update Posted:
2009-12-29
First Post:
2005-03-15
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Memory Aid for Informed Consent in Alzheimer's Research
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D000544', 'term': 'Alzheimer Disease'}], 'ancestors': [{'id': 'D003704', 'term': 'Dementia'}, {'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D024801', 'term': 'Tauopathies'}, {'id': 'D019636', 'term': 'Neurodegenerative Diseases'}, {'id': 'D019965', 'term': 'Neurocognitive Disorders'}, {'id': 'D001523', 'term': 'Mental Disorders'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED'}, 'enrollmentInfo': {'count': 110}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2004-09'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2009-12', 'completionDateStruct': {'date': '2007-03', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2009-12-23', 'studyFirstSubmitDate': '2005-03-15', 'studyFirstSubmitQcDate': '2005-03-15', 'lastUpdatePostDateStruct': {'date': '2009-12-29', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2005-03-16', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2007-03', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'MacArthur Competency Assessment Tool for Clinical Research (MacCAT-CR) to quantify decision making abilities'}], 'secondaryOutcomes': [{'measure': 'Participant competency'}]}, 'conditionsModule': {'keywords': ['Informed Consent', 'Memory Aid'], 'conditions': ["Alzheimer's Disease", 'Aging']}, 'referencesModule': {'references': [{'pmid': '7575221', 'type': 'BACKGROUND', 'citation': "Marson DC, Ingram KK, Cody HA, Harrell LE. Assessing the competency of patients with Alzheimer's disease under different legal standards. A prototype instrument. Arch Neurol. 1995 Oct;52(10):949-54. doi: 10.1001/archneur.1995.00540340029010."}, {'pmid': '11329391', 'type': 'BACKGROUND', '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."}, {'pmid': '7955902', 'type': 'BACKGROUND', 'citation': 'Sachs GA, Stocking CB, Stern R, Cox DM, Hougham G, Sachs RS. Ethical aspects of dementia research: informed consent and proxy consent. Clin Res. 1994 Oct;42(3):403-12. No abstract available.'}, {'pmid': '12473015', 'type': 'BACKGROUND', 'citation': "Karlawish JH, Casarett DJ, James BD. Alzheimer's disease patients' and caregivers' capacity, competency, and reasons to enroll in an early-phase Alzheimer's disease clinical trial. J Am Geriatr Soc. 2002 Dec;50(12):2019-24. doi: 10.1046/j.1532-5415.2002.50615.x."}, {'type': 'BACKGROUND', 'citation': 'Appelbaum PS, Grisso T. The MacArthur Competence Assessment Tool - Clinical Research. Sarasota, FL: Professional Resources Press, 2000.'}, {'pmid': '20808101', 'type': 'DERIVED', 'citation': 'Rubright J, Sankar P, Casarett DJ, Gur R, Xie SX, Karlawish J. A memory and organizational aid improves Alzheimer disease research consent capacity: results of a randomized, controlled trial. Am J Geriatr Psychiatry. 2010 Dec;18(12):1124-32. doi: 10.1097/JGP.0b013e3181dd1c3b.'}]}, 'descriptionModule': {'briefSummary': "The purpose of this trial is to test whether a memory and organizational aid in the form of a document that summarizes and simplifies a study's key points can improve the decision-making abilities and competency of mild to early moderate Alzheimer's disease (AD) patients.", 'detailedDescription': "Studies of mild to moderate Alzheimer's disease (AD) patients reveal substantial variation in their ability to participate in an informed consent process. No published data show techniques that help an AD patient to participate in an informed consent. This research will address this issue by performing a randomized trial to test whether a memory and organizational aid can improve the decision-making abilities and competency of AD patients.\n\nThis study will recruit 80 patients with mild to early moderate AD, and 30 non-demented elderly persons. The informed consent protocol for a hypothetical early-phase drug trial will be administered by a trained interviewer in the patient's home. The AD patients will be randomized to receive either the standard informed consent process or the intervention of the standard informed consent process plus the memory and organizational aid. All non-demented elderly individuals will receive the standard informed consent process. The interviewer will administer the protocol to participants and ask questions that will assess participant capacity to understand, appreciate, reason, and make a choice concerning enrollment in the hypothetical study."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Live within one hour drive of the University of Pennsylvania's Memory Disorders Clinic\n* Education equivalent to 6th grade level\n* Corrected visual acuity of at least 20/70\n* Speak English\n* Diagnosed with possible or probable AD, or non-demented\n* MMSE (Mini Mental State Exam) \\>= 18"}, 'identificationModule': {'nctId': 'NCT00105612', 'briefTitle': "Memory Aid for Informed Consent in Alzheimer's Research", 'organization': {'class': 'NIH', 'fullName': 'National Institute on Aging (NIA)'}, 'officialTitle': "Improving Informed Consent in Alzheimer's Disease Research", 'orgStudyIdInfo': {'id': 'IA0070'}, 'secondaryIdInfos': [{'id': '1R01AG020627-01A2', 'link': 'https://reporter.nih.gov/quickSearch/1R01AG020627-01A2', 'type': 'NIH'}]}, 'armsInterventionsModule': {'interventions': [{'name': 'Memory and Organizational Aid', 'type': 'DEVICE'}, {'name': 'Standard Informed Consent Process', 'type': 'BEHAVIORAL', 'description': "The informed consent protocol for a hypothetical early-phase drug trial will be administered by a trained interviewer in the patient's home"}]}, 'contactsLocationsModule': {'locations': [{'zip': '19104', 'city': 'Philadelphia', 'state': 'Pennsylvania', 'country': 'United States', 'facility': 'University of Pennsylvania, Memory Disorders Clinic', 'geoPoint': {'lat': 39.95238, 'lon': -75.16362}}], 'overallOfficials': [{'name': 'Jason Karlawish, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Pennsylvania Institute on Aging'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'National Institute on Aging (NIA)', 'class': 'NIH'}}}}