Improving cognition in severe mental illness by combining cognitive remediation and transcranial direct current stimulation: study protocol for a pragmatic randomized controlled pilot trial (HEADDSET)

被引:4
|
作者
Poppe, Anika [1 ,2 ]
Bais, Leonie [1 ]
van Duin, Danielle [3 ,4 ]
Curcic-Blake, Branislava [5 ]
Pijnenborg, Gerdina Hendrika Maria [2 ,6 ]
van der Meer, Lisette [1 ,2 ]
机构
[1] Lentis Psychiat Inst, Dept Rehabil, Lagerhout E35, NL-9741 KE Zuidlaren, Netherlands
[2] Univ Groningen, Dept Clin & Dev Neuropsychol, Grote Kruisstr 2-1, NL-9712 TS Groningen, Netherlands
[3] Trimbos Inst, Utrecht, Netherlands
[4] Phrenos Ctr Expertise, Utrecht, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Sci Cells & Syst, Cognit Neurosci Ctr, Groningen, Netherlands
[6] GGZ Drenthe, Dept Psychot Disorders, Assen, Netherlands
关键词
Cognitive remediation training; Transcranial direct current stimulation; Social and functional recovery; Severe mental illness; Deinstitutionalization; Randomized controlled trial; SYNDROME SCALE PANSS; FUNCTIONAL-CAPACITY; NEGATIVE SYMPTOMS; SCHIZOPHRENIA; HEALTH; TDCS; METAANALYSIS; PLASTICITY; COMMUNITY; ACCEPTABILITY;
D O I
10.1186/s13063-021-05230-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundA fundamental challenge for many people with severe mental illness (SMI) is how to deal with cognitive impairments. Cognitive impairments are common in this population and limit daily functioning. Moreover, neural plasticity in people with SMI appears to be reduced, a factor that might hinder newly learned cognitive skills to sustain. The objective of this pilot trial is to investigate the effects of cognitive remediation (CR) on cognitive and daily functioning in people dependent on residential settings. In addition, transcranial direct current stimulation (tDCS) is used to promote neural plasticity. It is expected that the addition of tDCS can enhance learning and will result in longer-lasting improvements in cognitive and daily functioning.MethodsThis is a pragmatic, triple-blinded, randomized, sham-controlled, pilot trial following a non-concurrent multiple baseline design with the participants serving as their own control. We will compare (1) CR to treatment as usual, (2) active/sham tDCS+CR to treatment as usual, and (3) active tDCS+CR to sham tDCS+CR. Clinical relevance, feasibility, and acceptability of the use of CR and tDCS will be evaluated. We will recruit 26 service users aged 18years or older, with a SMI and dependent on residential facilities. After a 16-week waiting period (treatment as usual), which will serve as a within-subject control condition, participants will be randomized to 16 weeks of twice weekly CR combined with active (N=13) or sham tDCS (N=13). Cognitive, functional, and clinical outcome assessments will be performed at baseline, after the control (waiting) period, directly after treatment, and 6-months post-treatment.DiscussionThe addition of cognitive interventions to treatment as usual may lead to long-lasting improvements in the cognitive and daily functioning of service users dependent on residential facilities. This pilot trial will evaluate whether CR on its own or in combination with tDCS can be a clinically relevant addition to further enhance recovery. In case the results indicate that cognitive performance can be improved with CR, and whether or not tDCS will lead to additional improvement, this pilot trial will be extended to a large randomized multicenter study.Trial registrationDutch Trial Registry NL7954. Prospectively registered on August 12, 2019.
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页数:16
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