Aging Clinical Trial
Official title:
Comprehensive Cognitive Remediation as a Strategy to Prevent Cognitive Impairment Associated With Age and Disability in the Elderly With the REHACOP Program
NCT number | NCT03435029 |
Other study ID # | NSMC-004-UD |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2012 |
Est. completion date | March 2018 |
Verified date | July 2019 |
Source | University of Deusto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of the study was to analyze the effectiveness of a comprehensive cognitive
remediation program (REHACOP) in the non demented elderly, obtaining improvements in
cognition and functional skills. It was a longitudinal randomized controlled trial with three
assessments: basal, post-treatment, and 12-month follow-up.
Recruitment and enrollment were conducted between September 2012 and November 2016. All
participants underwent a clinical interview and an extensive neuropsychological battery.
Patients were randomized in an experimental and a control group. The groups were formed by a
maximum of eight participants run by an experienced therapist. The experimental group
received cognitive remediation for 3 months, 3 times per week, 60 minutes per session. The
control group consisted of occupational group activities (reading the newspaper, drawing,
singing or doing crafts) with the same frequency as the experimental group. Post-treatment
assessment was carried out within the first week after completing the intervention. Finally,
longitudinal follow-up at 12 months with neuropsychological assessments will be performed.
Objective: To examine the efficacy of a comprehensive cognitive training program (REHACOP) to
improve cognition, clinical symptoms and functional disability for the elderly.
Status | Completed |
Enrollment | 140 |
Est. completion date | March 2018 |
Est. primary completion date | February 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 55 Years and older |
Eligibility |
Inclusion Criteria: 1. age over 55 years 2. signing informed consent 3. independence in daily living activities Exclusion Criteria: 1. history of neurological or psychiatric conditions, Neuropsychiatric Inventory Cummings > 4 2. illiterate 3. Mini Mental State Examination < 20 4. severe physical constraints. |
Country | Name | City | State |
---|---|---|---|
Spain | University of Deusto | Bilbao | Bizcay |
Lead Sponsor | Collaborator |
---|---|
University of Deusto |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline to post-treatment and follow-up on one final neurocognition composite score after receiving cognitive remediation. | The neurocognition composite score is one z score that was based on the following test: BTA total score, total score of the forward digits and backward digit of the WAIS-III, total number of words beginning with the letter "p" in 3-minute and total number of words for animals and supermarket categories in 1-minute of the CIFA, total score of learning and total score of long-term recall of the HVLT-R, total score of learning and long-term recall of the BVMT-R, total score of the free drawing of the CDT, total score of letters and total score of the cube analysis of the VOSP, time of the TMT-A, total score of the SPCT, and total score of the word-color trial of the Stroop Test. All raw scores were converted to z-scores. TMT-A score was adjusted so that higher scores indicated better performance. The z-scores were pooled into one composite score with the average of the primary measures mentioned above. Higher scores in this composite score indicated better performance. | 3 months and 12 months follow-up | |
Secondary | Change from baseline score to post-treatment and follow-up on Geriatric Depression Scale (GDS) | Geriatric Depression Scale (GDS-15) includes 15 items. Higher scores indicate a higher degree of depression (range from 0 to 15 points). | 3 months and 12 month follow-up | |
Secondary | Change from baseline score to post-treatment and follow-up on Neuropsychiatric Inventory Questionnaire (NPI-Q) | Neuropsychiatric Inventory Questionnaire (NPI-Q) includes 10 neuropsychiatric (delusions, hallucinations, agitation/aggression, depression/dysphoria, anxiety, euphoria, apathy, disinhibition, irritability, and aberrant motor behavior) domains assessed in terms of severity and frequency in a range from 0 to 120 points. Higher scores indicate greater neuropsychiatric behaviors. | 3 months and 12 months follow-up | |
Secondary | Change from baseline score to post-treatment and follow-up on Lille Apathy Rating Scale (LARS) | Lille Apathy Rating Scale (LARS) is composed by 33 items, subdivided into 9 subscales (everyday productivity, interests, taking initiative, novelty seeking/motivation, emotional responses, concern, social life, and self-awareness). These subscales are summed into a total score with a possible range from -36 to 36 points. Lower scores indicate a higher degree of apathy. | 3 months and 12 months follow-up | |
Secondary | Change from baseline score to post-treatment and follow-up on Multidimensional Fatigue Inventory (MFI) | Multidimensional Fatigue Inventory (MFI) is composed by 20 items divided into 5 subscales (general index, physical fatigue, mental fatigue, lack of motivation, lack of activity). Higher scores indicate greater fatigue (range from 0 to 140 points). | 3 months and 12 months follow-up | |
Secondary | Change from baseline score to post-treatment and follow-up on Satisfaction With Life Scale (SWLS) | Satisfaction With Life Scale (SWLS). This scale is composed by 5 items. Higher scores indicate greater live satisfaction (range from 0 to 35 points) | 3 months and 12 months follow-up | |
Secondary | Change from baseline score to post-treatment and follow-up on Subjective Questionnaire on Cognitive and Functional Difficulties of the patient and caregivers | Subjective complains were assessed by Subjective Questionnaire on Cognitive and Functional Complains of the patient and caregivers. These questionnaires are composed by 40 items each one of them. Higher scores indicate greater subjective complains (range from 0 to 120 points). | 3 months and 12 months follow-up |
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