group factor and intervention as a between-groups
factor. Effect sizes were determined with Cohen’s d
(the mean change score divided by the pooled
standard deviation).
The results of pretreatment comparison
suggested relatively stable cognitive functions in
both groups during the first (pretreatment) phase of
the experiment. The two groups exhibited similar
effect sizes.
Post-treatment comparisons generally revealed
improved cognitive performance and higher effect
sizes in both groups. In six outcome measures, the
tDCS group performed better than the sham group.
Importantly however, none of the differences
between groups were statistically significant.
At the 4-month follow-up, both groups showed
improved performance in most tests (compared to
pre-treatment), as indicated by the increases in effect
sizes. The tDCS group achieved higher effect sizes
than the sham group in five outcome measures.
However, the differences between the groups were
not sufficiently marked to reach the significance
level.
5 DISCUSSION
In this study, we hypothesized that consecutive A-
tDCSs would facilitate adaptive changes in neural
networks that were involved in attention control and
memory track formation. We assumed that these
changes would strengthen the effects of the
cognitive training.
Our results did not provide sufficiently strong
evidence to support the use of repeated A-tDCS over
the left DLPFC for neuromodulation supplementary
to cognitive rehabilitation of individuals recovering
from severe TBI. However, since the tDCS-treated
group exhibited overall larger effects sizes, some
positive response to stimulation may be possible. It
is likely that longer and/or more intense stimulation
as well as better control of EEG activity (Ulam et
al., 2014) will result in more beneficial effects in
future studies.
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MEDLINE, EBSCOhost, viewed 18 August 2014