Table 3. Summary characteristics of studies on remotely-delivered cognitive remediation and cognitive training.
Authors (Year) | Disease | N/Group Condition | Age (SD) | Design | Number of Sessions/ Period | Setting (Individual/Group/ Couple) | Outcome Measures | Results |
---|---|---|---|---|---|---|---|---|
Anguera et al. (2017) | Sensory Processing Dysfunction (SPD) | Experiment 1 = 62 (20 SPD +ADHD, 25 Control & 17 SPD only) | 9.7 (1.3) SPD +ADHD, 10.5(1.3) Healthy Control, 10.3(1.5) SPD | Pilot Study; experimental design | 30 mins per day which consists of 7 tasks, 3–4 minutes sessions, 5 days per week for 4 weeks | Patient (a child) and their caregiver (parent) | Perceptual discrimination task, Test of Variables of Attention (TOVA) & EVO assessment (perceptual discrimination, visuomotor tracking and multitasking ability) |
|
Experiment 2 = 57 (Final analysis:17, 22 & 10) | ||||||||
Boman et al. (2004) | Mild to moderate acquired non-progressive brain injury | 10 | 47.5 | Pre-post-follow-up design (single group) | 1 hour, three times weekly for 3 weeks in their home or at work | Individual | The Attention Process Training test, Digit Span Test, Claeson-Dahl test, The Rivermead Behavioural Memory test, The Assessment of Motor and Process Skills, The European Brain Injury Questionnaire, Self-perceived quality of life. | Significant improvement in attention, concentration and memory.
|
Caller et al. (2016) | Epilepsy | 66 randomized to 3 equal groups. Final analysis: 15 in H, 14 in H+ (coupled with memory training) and 20 control | 49.3(9.2) H/H+ and 41.4(11.2) control | Randomized control trial | 20–40 min daily, 5 days a week for 8 weeks | Individual | Quality of Life in Epilepsy scale, QOLIE-31, RBANS, PHQ-9, FACT-Cog, BRIEF-A and Satisfaction Survey | Significant improvement in cognition and quality of life. |
Charvet et al. (2015) | Multiple Sclerosis | 20 (11 Experiment & 9 Active Control) | 19–55 | Double blind randomized control trial | 30 min per day/5 days a week over 12 weeks (Target: 60 total days played across 3 months) | Individual |
Cognitive Composite:
|
Significant improvement in cognitive measures and motor tasks. |
Motor Composite:
| ||||||||
Self-report measures:
| ||||||||
Charvet et al. (2017) | Multiple Sclerosis | 135 (74 Experiment & 61 Active control) | 50 (12) | Double blind randomized control trial | 1 hour per day, 5 days a week over 12 weeks (Total target: 60 hours) | Individual | Neuropsychological Test–PASAT, WAIS-IV (LNS & DSB), BVMT-R, D-KEFS, (2) Self Report change in Cognition. | Significant improvement in cognitive functioning. |
Cody et al. (2015) | HIV | 20 | 50.22(6.57) | Within subjects pre-post experiment | 2 hours per week for 5 weeks (Target is 10 hours) | Individual | Useful Field of View (UFOV®) Wisconsin Card Sorting, Finger Tapping, Timed IADL measures and feedback on training | Significant improvement in processing speed and possible transfer to activity of daily living. |
Fisher et al. (2009) | Schizophrenia | 55 (29 experiment auditory training & 26 control- computer games)
|
Experiment 42.86 (10.07) |
Pre-post; controlled experiment design | 1 hour per day, 5 days per week for 10 weeks | Individual | PANSS, Quality of Life–Abbreviated Version and MATRICS |
|
Control 45.31(9.39) | ||||||||
Fisher et al. (2015) | Schizophrenia | 86 (43 experiment & 43 Control group) | 21.22 | Double blind randomized control trial | 1 hour daily, 5 days per week for 8 weeks (40 hours training) | Individual | MATRICS, D-KEFS Tower Test, Strauss Carpenter Outcome, and Global Functioning: Role and Social Scales | Participants in experiment group (auditory training) showed significant improvement in cognition, memory and problem solving. |
Johnstone et al. (2017) | ADHD | Total 107; 54 experiment (44 completed) & 53 control (41 completed) | N/A | Randomized waitlist control design | 25 sessions over a period of 6 to 8 weeks (3 or 4 sessions a week) | Patient (child) and their caregiver (parent) | CBCL, Conners 3-P, ADHD-RS, and WIAT-11 | Trainees improved in the trained tasks but enjoyment and engagement declined. |
Kirk et al. (2016) | Intellectual and developmental disabilities (IDD) | 76 (38 Experiment & 38 Control; 37 in final analysis | 8.22 | Double blind randomized control trial | About 20 min per day, 5 times per week, over a 5 week period | Patient (a child) and their caregiver (parent) | WATT and SWAN | Children that received home based attention training showed greater improvement in selective attention performance. |
Loewy et al. (2016) | Clinical High Risk (CHR) patients for psychosis | 83 (Experiment 50; only 31 completed & Control 33; only 17 completed) | 18.1 | Double blind randomized control trial | 1 hour per day, 5 days a week for 8 weeks (40 hours total) | Individual | SOPS, Global Functioning: Role and Social Scales, MATRICS, D-KEFS, NAB Mazes, HVLT-R and BVMT-R | Participants in experiment group showed significant improvement in verbal memory. |
Mariano et al. (2015) | 22q11 Deletion Syndrome | Enrolled: 22 Final analysis: 21 | 14.6 (1.3) | Longitudinal within-group design | 45 min per day, 3 times per week for 8 months | Individual (teleconference) | Neurocognitive test battery; CNS Vital Signs (CNS-VS) | Significant improvement in working memory, shifting attention and cognitive flexibility. |
McBride et al. (2017) | Chronic Fatigue Syndrome (CFS) | 76 (36 CBT/GET program & 36 CBT/ GET + CR program) | 35.5 (age range: 13–71) | Case control trail | 3–5 sessions per week, up to a total of 40 sessions | Individual | SPHERE (SOMA & PSYCH subscale), SF-36, Neuropsychological Performance measures | Significant improvement in neurocognitive symptoms and cognition. |
Milman et al. (2014) | Parkinson’s Disease | 18 | 67.7 (6.4) | Pre-post; single group experiment | 30 min a day, 3 days per week for 12 weeks | Individual | The Mindstreams (NeuroTrax Corp., TX) battery of computerized neuropsychological test and the Timed Up and Go (TUG) test | Significant improvement in global cognitive score & Timed Up and Go (TUG) measures. |
Mohanty & Gupta (2013) | Traumatic Brain Injury (TBI) | 1 | 24 | Single case study | 45 min to 1 hour twice a day, for 9 months | Individual and parent (father) | PGI Battery of Brain Dysfunction, Selected tests from NIMHANS & Dysfunctional Analysis Questionnaire | Improvement in cognitive functions and day to day functioning. |
Nahum et al. (2014) | Schizophrenia | 34 (17 Schizophrenia & 17 matched healthy control) | 23.7 | Pilot experimental study & within subject design | 1–2 hours per day, 2–5 days per week for 6–12 weeks (24 hours) | Individual | SocialVille Training Program Feasibility and ease of use, SocialVille Exercise-based Assessments, Penn Facial Memory, PROID, MSCEIT), Social and Role Scales, SFS, QLS, BIS/BAS, TEPS | Improvement on speeded SocialVille and working memory tasks, motivation, social cognition and functioning.
|
Pyun et al. (2009) | Stroke (Cognitive Impairment) | Recruited 6 (2 did not complete the full 12 week home program) | 48.7 (age range 28–62) | Multiple case study | 2 hours (only 30 min of CR) per day, 7 days a week for 12 weeks | Patients and their caregivers | MMSE, NCSE, domain-specific computerized neuropsychological test, LOTCA, MBI & S-IADL | Significant improvement in activity of daily living and marginal improvement in general cognition. |
Quayhagen et al. (2001) | Alzheimer’s Dementia |
Experiment 1 56 couples (experimental vs. placebo vs. control) |
Experiment 1 Patients; 73.18 & caregivers 67.75 |
Randomized control trial |
Experiment 1 1 hour a day, 5 days a week for 12 weeks. |
Spousal-caregiving units (patient and caregiver) | WMS-R, DRS, FAS, GCS & Marital Needs Satisfaction Scale. | Improvement in immediate memory for experimen1 and problem solving for experiment 2. Verbal fluency improved in both studies. |
Experiment 2 Patients; 74.97 & caregiver 72.57 |
Experiment 2 30 couples (experiment vs. control) |
Experiment 2 1 hour a day, 5 days a week for 8 weeks. |
||||||
Quayhagen et al. (1995) | Alzheimer’s Dementia | 79 patients and caregivers (78 in final analysis) | 73.6 (8.0) patients & 66.7 (10.8) caregivers | Randomized control trial | 1 hour a day, 6 days a week for 12 weeks | Patient and their caregiver | DRS, WMS-R, FAS, Geriatric Coping Schedule, Memory and Behavior Problems Checklist (part A) | Experiment group showed improvement in cognition and behavioral performance. |
Rajeswaran et al. (2017) | Schizophrenia | 1 | 26 | Pre-post intervention single case study | 1 hour a day for 10 weeks | Individual (patient) and caregiver (mother) | NIMHANS & social functioning | Cognitive retraining improved cognitive functions. |
Regan et al. (2017) | Mild Cognitive Impairment (MCI) & Alzheimer’s Dementia (AD) | 55 enrolled; 40 finished study (25 intervention & 15 control) | Client: 77.2 (6.5), Caregiver: 66.8 (15.0) | Multicenter randomized control trail | 1 hour per week for 4 weeks | Individual with their caregiver | COPM, HADS, ICQ, MMCQ, QOD, B-ADL, ECOQ, RMBPC | Intervention group showed significant improvement in performance and satisfaction. |
Shaw et al. (2017) | Multiple Sclerosis (MS) and Parkinson Disease (PD) | Study 1: 26 (MS) | N/A | Study 1: Open label | Study 1: 20 min per day, 5 days a week for two weeks (9 session at home) | Individual | Feasibility report, UPDRS, NSNQ, PROMIS & PANAS |
|
Study 2: Double blind randomized sham control study (PD arm open label) | Study 2: 20 (MS) & 6 (PD) | Study 2 = 20 & PD = 10 | ||||||
Vazquez-Campo et al. (2016) | Schizophrenia | 21 (12 intervention & 9 control); final = analysis 19 | 39.28 | Pre/post pilot study | 1 hour per week for 12 weeks | Individual | EP; Ekman 60 Faces Test, ToM; Hinting Task, Recognition of Faux Pas, Strange Stories of Happe, AIHQ; Ambiguous Intentions Hostility Questionnaire, MSCEIT, PANSS, WAIS-IV & Semi-structured interview | Significant improvement in EP, ToM and AS variables.
|
Ventura et al. (2013) | Schizophrenia | Recruited 9 (8 completed study) | N/A | Feasibility study | 1 hour twice per week for 6 weeks | Individual and relative |
|
Improvement in cognition, knowledge (about the role of cognition in daily life), and improvement in social functioning. |