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Table 1 RESULTS
Prior to initiating the experimental
protocol, 6 groups of normal subjects were studied to determine the drumming
approach to be used for the treatment group. Tests of proportions (Figure
1 and Table 1) were used to determine the proportion of subjects whose measured
parameters were modulated in the predicted direction. The binomial test
was performed to elucidate statistically significant trends of post-pre
cortisol, NK cell activity, and DHEA-cortisol changes that occurred in a
direction opposite to that expected to be associated with the classic stress
response. NK cell activity was calculated as an arithmetic average of the
post- minus pre- differences for all NK cell activity and LAK cell activity
measures as well as E:T ratios to demonstrate a combined trend. Although
all parameters reported in the actual study also were analyzed in the preliminary
groups, it was determined that the "composite drumming" intervention
was the only protocol that demonstrated NK cell activity enhancement in
conjunction with appropriate hormonal responses (Table 1), and would thereby
be used as the treatment protocol for the actual study. The
purpose of this study was to compare the biological effects of a single
group-drumming intervention on normal subjects compared with controls. Hypothetical
differences between treatment and control groups were tested across 12 biological
markers, first globally across all 12 biological |
markers with a Hotelling T2 (P<.0005), then individually with independent
t tests adjusted for multiple comparisons (Table 2).
Although measures for affective change
(ie, anxiety and depression), volume shifting (ie, hematocrit), and cell
demargination (ie, white blood cell count) showed pre-post differences,
these changes were in the same direction and magnitude for both the experimental
and control groups. This finding suggests that the unique experimental
milieu, rather than the treatment per se, affected these results. Therefore,
random assignment of subjects to the treatment and control groups was
successful in controlling for sampling bias in these areas. In addition,
the Sense of Coherence Scale by Antonovsky/25 (measured
once at the end of the experiment on each subject) showed no significant
difference between the treatment group (mean=158) and control group (mean=150).
Serum cortisol and, to a lesser extent,
DHEA—2 of the 12 designated biological markers—exhibited a
similar pattern of reaction to the general milieu (within-groups effect),
but not to the treatment (between-groups effect). However, for plasma
DHEA there was a notable trend toward a difference between the treatment
and control groups (P=.073). The DHEA-to-cortisol ratio showed a significant
increase for within-group effects in the experimental subjects (P=.036).
Six of 10 NK cell assays, when expressed
as mean normalized change, were significant for alpha levels adjusted
for multiple comparisons (Table 2). Specifically, NK cell activity at
E:T ratios of 6:1, 12:1, and IFN-y-stimulated LAK cell activity with associated
baselines for E:T ratios of 12:1 and 25:1 were significantly increased
in the treatment group compared with the control group (Table 2). The
other 4 assays (ie, NK cell activity at E:T ratios of 25:1 and 50:1 and
IL-2-stimulated LAK cell activity at E:T ratios of 12:1 and 25:1) showed
a similar pattern of normalized change (to a lesser degree of significance)
in response to treatment. In fact, each of the 10 NK cell measures with
differing E:T ratios increased above the preexperimental level (ie, the
mean normalized change >0) in the treatment group; 8 of 10 declined
slightly (ie, mean normal-ized change <0) in the control group (Figure
2).
Comparison of baselines for IFN-y-stimulated
LAK cell activi-ty at E:T ratios of 12:1 and 25:1 and for NK cell activity
at E:T ratios of 12:1 and 25:1 showed an enhanced sensitivity effect for
the 2 baselines due to their extended incubation times. Also, changes
in natural killing ability, especially when activated by IFN-y (eg, LAK
with IFN-Y at E:T 12:1), were highly significant and clearly associated
with the drumming activity. Although enhanced lymphokine activation of
NK cell activity was evident in vitro, no significant in vivo changes
in plasma cytokine levels were detected. Although it is possible that
the time points selected in this study may not have
reflected in vivo cytokine level alterations, it should also be noted
that marked variability in measurements of plasma IL-2 and IFN-y may have
precluded accurate in vivo assessments.
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