- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03712839
Cognitive-functional Evaluation of Anosognosia
Cognitive and Cerebral Mechanisms of Anosognosia in Patients With Acquired Brain Damage: New Evaluation Strategies Based on Daily Tasks
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The proposed protocol is composed by two ecological tools: The Cog-Awareness ADL Scale (ADL scale of metacognitive knowledge) and the Basic and Instrumental ADL performance based test (Awareness ADL), to identify the presence of cognitive deficits and anosognosia in patients with ABI always within the context of everyday life activities. One first specific aim is to test the convergent validity of the two proposed ecological tools with other traditional and validated measures usually used to assess similar cognitive processes and components of self-awareness. The second specific objective is to investigate the external validity of the ecological tools, by testing whether they are able to discriminate between acquired brain damage patients with and without anosognosia and a group of neurologically healthy participants on every component.
After conducting a literature review of the subject we found that this would be the first protocol developed to identify all these components in the same study.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Presence of an acquired brain damage objectively observed with medical reports.
- Cognitive deficits relative to executive functions and/or memory evaluated by the team of professionals who recruit participants in the hospital.
Exclusion Criteria:
- Presence of a serious visuoperceptual deficit that makes it difficult to complete the ADL tasks, evaluated by the team of professionals who recruit participants in the hospital.
- Presence of an understanding deficit (aphasia) evaluated by the team of professionals who recruit participants in the hospital.
- Presence of spatial neglect evaluated with line cancellation and line bisection tests.
- Presence of motor deficits in both upper limbs that impedes to complete the ADL tasks.
- Total score in MMSE<18
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Acquired Brain Injury group with anosognosia
People with presence of an acquired brain damage and cognitive deficits relative to executive functions and memory.
To determine the presence of anosognosia, patients must present an overestimation value of their capacities greater than 5 (>5) in the discrepancy index on the Patient Competency Rating Scale (PCRS) (Prigatano et al., 1998).
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The participants will be evaluated with a set of tools within the context of meaningful ADL.
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Acquired Brain Injury group without anosognosia
People with presence of an acquired brain damage and cognitive deficits relative to executive functions and memory.
These patients must present a score of < 5 on the PCRS Scale.
|
The participants will be evaluated with a set of tools within the context of meaningful ADL.
|
|
Control group
Healthy participants matched in age, gender and educational level with the others two groups.
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The participants will be evaluated with a set of tools within the context of meaningful ADL.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The awareness ADL
Time Frame: 30-45 minutes
|
Participants will be asked to do activities of daily living such as preparing a breakfast or dressing in which measures that evaluate components of anosognosia will be used. In the tasks of ADL conflict situations (and standardized solutions previously defined) and distractor objects will be presented. The total errors committed will be analyzed, as well as those committed only by conflict situations and distractor objects. The percentage of errors detected and corrected errors will be calculated. In addition, anticipatory awareness, self-evaluation and updating processes will be examined. |
30-45 minutes
|
|
The Cog-Awareness ADL Scale
Time Frame: 10-15 minutes
|
For the aim of this study, the Cog-Awareness ADL Scale, will have two versions, one to be administered to a direct caregiver and the other to the patient to observe the discrepancy index in relation to functionality-cognition.
This tool allow to evaluate eight key cognitive abilities-task: manipulation difficulties, action schema, distraction, substitution, repetition, error detection, problem solving and task self-initiation in the two basic ADL and in the two instrumental ADL (BADL and IADL, respectively) (34 items).
Both patients and caregivers must answer how often the patients present this cognitive-functional error in each of the 4 ADLs: 1: never, 2: sometimes, 3: quite often and 4: always.
Two indices are calculated, one for BADL and one for IADL, adding all the scores of the two activities of each category among the number of activities answered.
Lower punctuation is interpreted with worse results.
There are 3 items that your scores should be reversed.
|
10-15 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mini-Mental State Examination
Time Frame: 10 minutes
|
General cognitive status.
MMSE is a 30-point questionnaire that is used extensively in clinical and research settings to measure cognitive impairment.
It is commonly used in medicine and allied health to screen for dementia.
It is also used to estimate the severity and progression of cognitive impairment and to follow the course of cognitive changes in an individual over time; thus making it an effective way to document an individual's response to treatment.
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10 minutes
|
|
Line cancellation test
Time Frame: 3-5 minutes
|
General cognitive status.
In the LCT the patient is asked to cross out all the lines (or particular items) on a sheet.
|
3-5 minutes
|
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Line bisection test
Time Frame: 3-5 minutes
|
General cognitive status.
The LBT is a quick measure to detect the presence of unilateral spatial neglect (USN).
To complete the test, one must place a mark with a pencil through the center of a series of horizontal lines.
Usually, a displacement of the bisection mark towards the side of the brain lesion is interpreted as a symptom of neglect.
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3-5 minutes
|
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Key search test
Time Frame: 2-4 minutes
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Executive functions.
Participants are required to search for an imaginary key they have lost on a field (a square on a piece of paper).
By drawing their search route, an indication of search strategy and planning ability can be deduced.
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2-4 minutes
|
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INECO Frontal Screening
Time Frame: 6-10 minutes
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Executive functions.
This screening test was designed to provide health professionals with a sensitive and specific executive screening test to determine frontal dysfunction in patients with dementia.
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6-10 minutes
|
|
Color trail making
Time Frame: 6 minutes
|
Executive functions.
Numbered circles are printed with vivid pink or yellow backgrounds that are perceptible to colorblind individuals.
For Part 1, the respondent uses a pencil to rapidly connect circles numbered 1-25 in sequence.
For Part 2, the respondent rapidly connects numbered circles in sequence, but alternates between pink and yellow.
The length of time to complete each trial is recorded, along with qualitative features of performance indicative of brain dysfunction, such as near-misses, prompts, number sequence errors, and color sequence errors.
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6 minutes
|
|
Rey Auditory Verbal Learning Test
Time Frame: 10-15 minutes
|
Semantic and episodic memory.
The RAVLT evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, learning strategies, retroactive, and proactive interference, presence of confabulation of confusion in memory processes, retention of information, and differences between learning and retrieval.
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10-15 minutes
|
|
Patient Competency Rating Scale
Time Frame: 6-10 minutes
|
Metacognitive knowledge. The primary purpose of the PCRS is to evaluate self-awareness (the ability to appraise one's current strengths and weaknesses) following traumatic brain injury. The PCRS is a 30-item self-report instrument which asks the subject to use a 5-point Likert scale to rate his or her degree of difficulty in a variety of tasks and functions. The subject's responses are compared to those of a significant other (a relative or therapist) who rates the subject on the identical items. Impaired self-awareness may be inferred from discrepancies between the two ratings, such that the subject overestimates his/ her abilities compared to the other informant. Awareness of deficit may also be examined separately for activities of daily living, behavioral and emotional function, cognitive abilities, and physical function. Range Discrepancy index range 1-150. Mean healthy subjects: 144 range (120-150) and relatives 145 (range 134-150) (Prigatano, 1998) |
6-10 minutes
|
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Verbal Fluency Test
Time Frame: 5 minutes
|
In this test the participants have to produce as many words as possible from a category in a 60 seconds.
This category is semantic (animals) and phonemic, including words beginning with F, A and S.
|
5 minutes
|
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Weekly Calendar Planning Activity (WCPA)
Time Frame: 20 minutes
|
This is a performance based test that measures different executive functions, among which are: planning, problem solving, inhibition of non-relevant information and maintenance and monitoring of rules.
In its short version, it is based on asking the patient to schedule 10 appointments (that appear in random order) during a 1 week span.
Some appointments are incompatible with others, so the patient has to take them into account to plan correctly.
In addition, the patient is asked to comply with 5 rules which are informed at the beginning of the test and are kept in view throughout the task.
The test provides different variables for its analysis, as well as the successes when planning, such as the types of mistakes made, the ability to detect them, the time, the rules followed or the strategies used.
|
20 minutes
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: María Jesús Funes-Molina, Professor, Facultad de Psicología (Departamento de Psicología Experimental) - Campus de Cartuja s/n, Granada, 18071
Publications and helpful links
General Publications
- Folstein MF, Folstein SE, McHugh PR. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975 Nov;12(3):189-98. doi: 10.1016/0022-3956(75)90026-6. No abstract available.
- Giovannetti T, Libon DJ, Hart T. Awareness of naturalistic action errors in dementia. J Int Neuropsychol Soc. 2002 Jul;8(5):633-44. doi: 10.1017/s135561770280131x.
- Prigatano GP, Bruna O, Mataro M, Munoz JM, Fernandez S, Junque C. Initial disturbances of consciousness and resultant impaired awareness in Spanish patients with traumatic brain injury. J Head Trauma Rehabil. 1998 Oct;13(5):29-38. doi: 10.1097/00001199-199810000-00005.
- Forde EM, Humphreys GW, Remoundou M. Disordered knowledge of action order in action disorganisation syndrome. Neurocase. 2004 Feb;10(1):19-28. doi: 10.1080/13554790490960459.
- Schmidt J, Fleming J, Ownsworth T, Lannin NA. Video feedback on functional task performance improves self-awareness after traumatic brain injury: a randomized controlled trial. Neurorehabil Neural Repair. 2013 May;27(4):316-24. doi: 10.1177/1545968312469838. Epub 2012 Dec 27.
- Rodriguez-Bailon M, Montoro-Membila N, Garcia-Moran T, Arnedo-Montoro ML, Funes Molina MJ. Preliminary cognitive scale of basic and instrumental activities of daily living for dementia and mild cognitive impairment. J Clin Exp Neuropsychol. 2015;37(4):339-53. doi: 10.1080/13803395.2015.1013022. Epub 2015 Mar 25.
- Forde EM, Humphreys GW. Dissociations in routine behaviour across patients and everyday tasks. Neurocase. 2002;8(1-2):151-67. doi: 10.1093/neucas/8.1.151.
- Sirigu A, Zalla T, Pillon B, Grafman J, Agid Y, Dubois B. Selective impairments in managerial knowledge following pre-frontal cortex damage. Cortex. 1995 Jun;31(2):301-16. doi: 10.1016/s0010-9452(13)80364-4.
- Sirigu A, Zalla T, Pillon B, Grafman J, Agid Y, Dubois B. Encoding of sequence and boundaries of scripts following prefrontal lesions. Cortex. 1996 Jun;32(2):297-310. doi: 10.1016/s0010-9452(96)80052-9.
- Torralva T, Roca M, Gleichgerrcht E, Lopez P, Manes F. INECO Frontal Screening (IFS): a brief, sensitive, and specific tool to assess executive functions in dementia. J Int Neuropsychol Soc. 2009 Sep;15(5):777-86. doi: 10.1017/S1355617709990415. Epub 2009 Jul 28. Erratum In: J Int Neuropsychol Soc. 2010 Sep;16(5):737.
- Toglia J, Kirk U. Understanding awareness deficits following brain injury. NeuroRehabilitation. 2000;15(1):57-70.
- Merchan-Baeza JA, Rodriguez-Bailon M, Ricchetti G, Navarro-Egido A, Funes MJ. Awareness of cognitive abilities in the execution of activities of daily living after acquired brain injury: an evaluation protocol. BMJ Open. 2020 Oct 26;10(10):e037542. doi: 10.1136/bmjopen-2020-037542.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PSI2016-80331-P
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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