Effectiveness of enhancing cognitive reserve in children, adolescents and young adults at genetic risk for psychosis: Study protocol for a randomized controlled trial
Offspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this project is to develop and investigate the efficacy of an intervention aimed at this population, based on the concept of cognitive reserve. This...
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Published in | Revista de psiquiatría y salud mental Vol. 16; no. 3; pp. 184 - 191 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Spain
Elsevier España S.L.U
01.07.2023
Elsevier España, S.L.U |
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Online Access | Get full text |
ISSN | 2950-2853 1888-9891 2950-2853 |
DOI | 10.1016/j.rpsm.2021.02.003 |
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Abstract | Offspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this project is to develop and investigate the efficacy of an intervention aimed at this population, based on the concept of cognitive reserve.
This is a multicenter randomized trial with an experimental test–retest design study with control group. Two groups will be included: a community comparison group (CC) and a Off-BDSZ group. A total of 108 Off-BDSZ and 65 CC aged between 6 and 25 years will be recruited. Off-BDSZ participants will be randomized to receive either Cognitive Reserve EnhAncement ThErapy (CREATE) (n=54), or a supportive approach (n=54). The CC group will be assessed at baseline. The duration of the intervention will be 3 months, with 12 weekly group sessions. The primary outcome will be the improvement in CR measured according to change in the Cognitive Reserve Assessment Scale in Health (CRASH) and Cognitive Reserve scale for Adolescents (CORE-A). All participants will be blindly evaluated using clinical, cognitive and neuroimaging measures at baseline, at three months (after the psychological intervention), and at twelve-month follow-up after treatment completion.
The results will provide insight into whether the CREATE-Offspring version may enhance cognitive reserve (CR) in child, adolescent and young adult Off-BDSZ as well as advance knowledge about changes in clinical manifestations, neuropsychological performance and brain structure and function associated with improving CR. This novel and cost-effective intervention represents an advance in the framework of preventive interventions in mental health.
Clinicaltrials.gov, NCT03722082. Registered on 26 October 2018. |
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AbstractList | AbstractBackgroundOffspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this project is to develop and investigate the efficacy of an intervention aimed at this population, based on the concept of cognitive reserve. MethodsThis is a multicenter randomized trial with an experimental test–retest design study with control group. Two groups will be included: a community comparison group (CC) and a Off-BDSZ group. A total of 108 Off-BDSZ and 65 CC aged between 6 and 25 years will be recruited. Off-BDSZ participants will be randomized to receive either Cognitive Reserve EnhAncement ThErapy (CREATE) ( n= 54), or a supportive approach ( n= 54). The CC group will be assessed at baseline. The duration of the intervention will be 3 months, with 12 weekly group sessions. The primary outcome will be the improvement in CR measured according to change in the Cognitive Reserve Assessment Scale in Health (CRASH) and Cognitive Reserve scale for Adolescents (CORE-A). All participants will be blindly evaluated using clinical, cognitive and neuroimaging measures at baseline, at three months (after the psychological intervention), and at twelve-month follow-up after treatment completion. DiscussionThe results will provide insight into whether the CREATE-Offspring version may enhance cognitive reserve (CR) in child, adolescent and young adult Off-BDSZ as well as advance knowledge about changes in clinical manifestations, neuropsychological performance and brain structure and function associated with improving CR. This novel and cost-effective intervention represents an advance in the framework of preventive interventions in mental health. Trial registrationClinicaltrials.gov, NCT03722082. Registered on 26 October 2018. Offspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this project is to develop and investigate the efficacy of an intervention aimed at this population, based on the concept of cognitive reserve. This is a multicenter randomized trial with an experimental test–retest design study with control group. Two groups will be included: a community comparison group (CC) and a Off-BDSZ group. A total of 108 Off-BDSZ and 65 CC aged between 6 and 25 years will be recruited. Off-BDSZ participants will be randomized to receive either Cognitive Reserve EnhAncement ThErapy (CREATE) (n=54), or a supportive approach (n=54). The CC group will be assessed at baseline. The duration of the intervention will be 3 months, with 12 weekly group sessions. The primary outcome will be the improvement in CR measured according to change in the Cognitive Reserve Assessment Scale in Health (CRASH) and Cognitive Reserve scale for Adolescents (CORE-A). All participants will be blindly evaluated using clinical, cognitive and neuroimaging measures at baseline, at three months (after the psychological intervention), and at twelve-month follow-up after treatment completion. The results will provide insight into whether the CREATE-Offspring version may enhance cognitive reserve (CR) in child, adolescent and young adult Off-BDSZ as well as advance knowledge about changes in clinical manifestations, neuropsychological performance and brain structure and function associated with improving CR. This novel and cost-effective intervention represents an advance in the framework of preventive interventions in mental health. Clinicaltrials.gov, NCT03722082. Registered on 26 October 2018. Offspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this project is to develop and investigate the efficacy of an intervention aimed at this population, based on the concept of cognitive reserve.BACKGROUNDOffspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this project is to develop and investigate the efficacy of an intervention aimed at this population, based on the concept of cognitive reserve.This is a multicenter randomized trial with an experimental test-retest design study with control group. Two groups will be included: a community comparison group (CC) and a Off-BDSZ group. A total of 108 Off-BDSZ and 65 CC aged between 6 and 25 years will be recruited. Off-BDSZ participants will be randomized to receive either Cognitive Reserve EnhAncement ThErapy (CREATE) (n=54), or a supportive approach (n=54). The CC group will be assessed at baseline. The duration of the intervention will be 3 months, with 12 weekly group sessions. The primary outcome will be the improvement in CR measured according to change in the Cognitive Reserve Assessment Scale in Health (CRASH) and Cognitive Reserve scale for Adolescents (CORE-A). All participants will be blindly evaluated using clinical, cognitive and neuroimaging measures at baseline, at three months (after the psychological intervention), and at twelve-month follow-up after treatment completion.METHODSThis is a multicenter randomized trial with an experimental test-retest design study with control group. Two groups will be included: a community comparison group (CC) and a Off-BDSZ group. A total of 108 Off-BDSZ and 65 CC aged between 6 and 25 years will be recruited. Off-BDSZ participants will be randomized to receive either Cognitive Reserve EnhAncement ThErapy (CREATE) (n=54), or a supportive approach (n=54). The CC group will be assessed at baseline. The duration of the intervention will be 3 months, with 12 weekly group sessions. The primary outcome will be the improvement in CR measured according to change in the Cognitive Reserve Assessment Scale in Health (CRASH) and Cognitive Reserve scale for Adolescents (CORE-A). All participants will be blindly evaluated using clinical, cognitive and neuroimaging measures at baseline, at three months (after the psychological intervention), and at twelve-month follow-up after treatment completion.The results will provide insight into whether the CREATE-Offspring version may enhance cognitive reserve (CR) in child, adolescent and young adult Off-BDSZ as well as advance knowledge about changes in clinical manifestations, neuropsychological performance and brain structure and function associated with improving CR. This novel and cost-effective intervention represents an advance in the framework of preventive interventions in mental health.DISCUSSIONThe results will provide insight into whether the CREATE-Offspring version may enhance cognitive reserve (CR) in child, adolescent and young adult Off-BDSZ as well as advance knowledge about changes in clinical manifestations, neuropsychological performance and brain structure and function associated with improving CR. This novel and cost-effective intervention represents an advance in the framework of preventive interventions in mental health.Clinicaltrials.gov, NCT03722082. Registered on 26 October 2018.TRIAL REGISTRATIONClinicaltrials.gov, NCT03722082. Registered on 26 October 2018. |
Author | Martinez-Aran, Anabel Solé, Brisa Serra-Blasco, Maria Castro-Fornieles, Josefina Vicent-Gil, Muriel Montejo, Laura Vieta, Eduard de la Serna, Elena Cardoner, Narcís Rosa-Justicia, Mireia Torrent, Carla Camprodon-Boadas, Patricia Sugranyes, Gisela |
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Keywords | SCQ ADHD DSM-V PAS CPT-II CREATE WCST ROCF Schizophrenia CHTE Bipolar disorder SCWT CAPE SCID CRASH WMS-III Core-A WASH-U-KSADS TOMAL Off-BD HDRS BPSS-P CC Cognitive reserve SLES CGI MAAS CPRS-48 TMT-A GAF CR fMRI WAIS-IV Offspring TMT-B CMRS Off-BDSZ WISC-IV SMR SOPS FAST K-SADS-PL YMRS Off-SZ SPQ-B questionnaire of habits and study techniques attention-deficit hyperactivity disorder Trail Making Test part-A Trail Making Test part-B Community Assessment of Psychic Experiences Offspring of patients diagnosed with schizophrenia Sexual Maturity Rating Global Assessment Functioning Conners’ Rating Scales 48 items Stroop Color-Word Interference Test Premorbid Adjustment Scale Test of memory and learning Cognitive Reserve EnhAncement ThErapy Cognitive Reserve scale for Adolescents Offspring of patients diagnosed with bipolar disorder and schizophrenia Cognitive Reserve Assessment Scale in Health structured clinical interview based on DSM-V Bipolar Prodrome Symptom Interview and Scale-Prospective functional magnetic resonance imaging Wechsler Memory Scale third edition Clinical Global Impressions Kiddie Schedule for Affective Disorders and Schizophrenia-Present – Lifetime Version community comparison group Schizotypal Personality Questionnaire-Brief Scale of Prodromal Symptoms Offspring of patients diagnosed with bipolar disorder Hamilton Depression Rating Scale for depressive symptomatology Child Mania Rating Scale Stressful Life Events Schedule Wechsler Intelligence Scale for Children fourth edition Cognitive Reserve Wechsler Adult Intelligence Scale fourth edition Continuous Performance Test second edition Mindful Attention Awareness Scale Functioning Assessment Short Test Kiddie Schedule for Affective Disorders and Schizophrenia version of university of Washington Rey-Osterrieth Complex Figure Social Communication Questionnaire Wisconsin Card Sorting Test Young Mania Rating Scale Diagnostic and Statistical Manual of Mental Disorders fifth edition |
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Snippet | Offspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness. The aim of this... AbstractBackgroundOffspring of patients diagnosed with bipolar disorder and schizophrenia (Off-BDSZ) have a high genetic risk of developing a mental illness.... |
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SubjectTerms | Adolescent Adult Bipolar disorder Bipolar Disorder - genetics Child Cognitive Reserve Humans Multicenter Studies as Topic Offspring Psychiatric/Mental Health Psychotic Disorders - genetics Randomized Controlled Trials as Topic Schizophrenia Schizophrenia - genetics Treatment Outcome Young Adult |
Title | Effectiveness of enhancing cognitive reserve in children, adolescents and young adults at genetic risk for psychosis: Study protocol for a randomized controlled trial |
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