2020 05 30 20117705 Full
2020 05 30 20117705 Full
2020 05 30 20117705 Full
Lillian Wieder, BSc1, Richard J. Brown, PhD, ClinPsyD2,3, Trevor Thompson, PhD4, & Devin B. Terhune,
PhD1
1
Department of Psychology, Goldsmiths, University of London, London, UK
2
School of Health Sciences, University of Manchester, Manchester, UK
3
Complex Trauma and Resilience Research Unit, Greater Manchester Mental Health NHS Foundation
Trust, Manchester Academic Health Sciences Centre, Manchester, UK
4
School of Human Sciences, University of Greenwich, London, UK
Corresponding author:
Devin B. Terhune, PhD
Department of Psychology
Goldsmiths, University of London
8 Lewisham Way
New Cross, London, UK SE14 6NW
d.terhune@gold.ac.uk
NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice.
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
Abstract
Objective Responsiveness to direct verbal suggestions (suggestibility) has long been hypothesized to
represent a predisposing factor for functional neurological disorder (FND) but previous research has yielded
conflicting results. The aim of this study was to quantitatively evaluate whether FND patients display
Methods Four electronic databases were searched in November 2019, with the search updated in April
2020, for original studies assessing suggestibility using standardized behavioural scales or suggestive
symptom induction protocols in FND patients and controls. The meta-analysis followed Cochrane,
PRISMA, and MOOSE guidelines. Data extraction and study quality coding were performed by two
protocols were used to calculate standardized mean differences (SMDs) between groups.
Results Of 26,643 search results, 19 articles presenting 11 standardized suggestibility datasets (FND:
n=316; control: n=360) and 11 symptom suggestibility datasets (FND: n=1285; control: n=1409) were
included in random-effects meta-analyses. Meta-analyses revealed that FND patients displayed greater
suggestibility than controls on standardized behavioural scales (SMD, 0.48 [95% CI, 0.15, 0.81]) and greater
responsiveness to suggestive symptom induction (SMD, 1.39 [95% CI, 0.92, 1.86]). Moderation analyses
presented mixed evidence regarding the extent to which effect sizes covaried with methodological
Conclusions These results corroborate the hypothesis that FND is characterized by heightened
responsiveness to verbal suggestion. Atypical suggestibility may confer risk for FND and be a cognitive
Introduction
Functional neurological disorder (FND) is characterized by impaired motor or cognitive functioning that
resembles neurological pathology but is not adequately explained by it.1 FND has a prevalence of 4-12 per
100,0002, 3 and represents ~16% of clinical referrals and visits to epilepsy clinics.4 It is associated with
considerable diagnostic delays and frequent misdiagnosis,5 which add to the already significant
FND has long been hypothesized to be characterized by elevated responsiveness to direct verbal
suggestions (suggestibility).7 Suggestibility is theorized to confer vulnerability for FND8 through aberrant
meta-awareness of intentions,9-12 the capacity for suggestions to trigger automatized behavioural routines or
mental representations,8 and/or a tendency to form precise (symptom) priors that override motor and
perceptual systems.13, 14 The use of suggestion to provoke FND symptoms is widely used to aid diagnosis15
and functional symptoms are responsive to suggestion-based treatments, such as hypnosis and placebo.16 In
addition, suggestibility has been shown to predict prognosis17 and response to treatment18 in FND patients.
Conditions with germane symptom profiles, such as dissociative disorders, are also characterized by
Despite these various strands of evidence, the empirical association between suggestibility and FND
seems to be highly variable.20, 21 In order to quantify the evidence for elevated suggestibility in FND
behavioural scales and in response to suggestive symptom induction protocols. Secondary analyses
methodological quality, the inclusion of a hypnotic induction,23 and symptom provocation method.15
Method
Eligibility criteria
Inclusion criteria included (1) English language; (2) full paper in a peer-reviewed journal; (3) patient sample
disorder (ICD), specific functional neurological syndromes (e.g., non-epileptic seizures), and conditions
where functional neurological symptoms are a diagnostic feature (i.e. DSM-IV somatization disorder;
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Briquet’s syndrome); (4) inclusion of a control group; and either (5) use of a standardized behavioural
measure of direct verbal suggestibility23, or (6) assessment of symptom induction through suggestion (e.g.,
Exclusion criteria included (1) studies in which suggestion was used to aid diagnosis; (2) case
suggestibility scales, which capture a different form of suggestibility characterized by high compliance24;
and (5) studies of patients with functional somatic syndromes not specifically characterized by functional
Search strategy
PubMed, PsycINFO, Web of Science and Academic Search Complete databases were searched in November
2019 for eligible studies using terms relating to suggestibility and FND (see online supplemental content
1) and then integrated into a single database. The search was repeated in April 2020 but yielded no new
studies. The reference lists of all eligible studies (and relevant review papers) were manually searched to
identify additional studies. Authors were contacted when data were unavailable or to clarify ambiguities in
methodology.
Study selection
Two raters (LW and a second rater) independently screened and assessed all studies for their eligibility using
a two-stage procedure. First, all titles and abstracts were screened and articles not meeting eligibility criteria
were rejected. Second, all remaining papers were reviewed to establish a final list of articles. Discrepancies
at either stage were resolved in consultation with a third reviewer (DBT) and sometimes a fourth reviewer
(RJB). Authors of eligible studies were contacted to address any questions regarding insufficient data. Of 5
author groups contacted, 4 (80%) provided data sufficient to permit study inclusion or answered queries that
justified exclusion.
Data extraction
The two outcome types (standardized suggestibility and symptom suggestibility) were measured using
continuous and categorical measures, respectively. After exclusion of two studies with overlapping data,
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It is made available under a CC-BY-NC-ND 4.0 International license .
data from eligible studies were extracted and coded independently by LW and the second rater using a data
extraction form including: (i) study details (title, year, geographical location), (ii) diagnosis, (iii), diagnosis
method, (iv) demographics (sample size and gender and age distributions), (v) study design details
method [live or recorded presentation], and scoring method [self or experimenter]), provocation method [see
Table 2], and experimenter blindness [blind, unblind, or unreported]), and (vi) descriptive statistics (Ms and
response counts include only responses identified as typical for the respective patient (typicality reported:
k=8; unreported: k=3). When studies reported results for more than one provocation method (k=2), the
rounded mean was used. Two studies included data for both standardized and symptom suggestibility. There
was 91% agreement between the two raters and discrepancies were resolved with a third reviewer (DBT).
Study quality
A 13-item scale was developed to assess study quality (see online supplemental content 1). Items were
adapted from an earlier meta-analysis that included items based on Cochrane criteria and PRISMA
recommendations25 and a range of other methodological criteria such as experimenter blindness. LW and the
second rater independently rated each item categorically (0=criterion not met, 1=criterion met) and a
summed total was computed for each study. Agreement between raters was 90% (kappa=.73) and
Individual study effect sizes included between-group differences in suggestibility that were computed with
standardised mean differences (SMDs; Hedges’s gs) using Review Manager (RevMan v. 5.3, 2014; The
Nordic Cochrane Centre, The Cochrane Collaboration, Copenhagen). Symptom suggestibility data consisted
of binary outcomes that were used to compute odds ratios, which were subsequently transformed to SMDs26
in MATLAB (v. 2017b, MathWorks, Natick, MA). SMDs were coded such that positive values reflected
Publication bias was assessed by examining funnel plots of effect sizes against standard errors for
asymmetry, as might occur due to a small number of studies with small or non-significant effect sizes. We
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(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
also tested for asymmetry using Egger’s bias test27 where p<.05 is indicative of asymmetry. We report
revised effect sizes correcting for asymmetry using the trim-and-fill method28 and funnel plots in
Figure 3.
Random-effects meta-analyses were performed in JASP (v. 0.8.6, 2019; JASP Team, Netherlands).
Outlier detection was made on the basis of studentized residuals (>|3.3|).29 There were no outliers in the
standardized suggestibility data (range: -1.63 to 1.33) or the symptom suggestibility data (range: -2.01 to
1.26). Moderating effects were assessed using meta-regression analyses whenever data were available for at
least 2 studies at each level of a categorical moderator and at least 10 studies for continuous moderators.30
Moderators included five categorical measures (experimenter blindness, hypnotic induction, symptom
provocation method [suggestion vs. nocebo; symptom studies], symptom typicality [not reported vs. report;
symptom studies]; and control type [non-clinical vs. clinical; standardized studies]) and one continuous
Results
Study inclusion
A PRISMA diagram showing study selection is presented in Figure 1. Principal features of these studies,
The 19 papers included 11 standardized suggestibility studies (FND: n=316, control: n=360) and 11
symptom suggestibility studies (FND: n=1285, control: n=1409). The standardized studies were published
between 1984 and 2009 and were conducted in the US (k=5), the Netherlands (k=4), and the UK (k=2). The
symptom studies were published between 1994 and 2018, and were conducted in the US (k=7), Puerto Rico
(k=1), France (k=1), India (k=1) and the UK (k=1). The mean percentage of females for standardized studies
was 86.13 for FND (k=8) and 45.71 for controls (k=7), whereas for symptom studies (k=6) it was 77.17 for
FND and 61.33 for controls. In the standardized studies, the mean age for FND was 31.22 (SD=8.01) (k=6),
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
and for controls it was 36.96 (SD=5.09) (k=7), whereas for the symptom studies (k=6), mean age for FND
Details of the types of standardized scales and provocation methods as well as the use of a hypnotic
induction are provided in Table 1 and Table 2, respectively. A hypnotic induction was used in 9
standardized studies and 3 symptom studies. All symptom studies included verbal suggestion but varied in
Ratings for each study on each of the 13 methodological quality criteria items are shown in online
supplemental content 1, Tables 1 and 2. Although some of the criteria were met by the majority of studies,
multiple criteria were not reliably met. Only 5 of 22 studies (23%) reported that the experimenter was blind
to group, 18 (82%) described the inclusion/exclusion criteria, 16 (73%) described the diagnosis procedure
and criteria in adequate detail, 10 (45%) described participant characteristics and 3 (14%) exhibited
demographic comparability between patients and controls. In the standardized studies, 7 of 11 (64%)
described the scale and procedure in adequate detail, and only 1 (9%) included a measure to correct for
compliance. In the symptom studies, 8 of 11 (73%) clearly described the provocation method.
Meta-analysis of 11 standardized behavioural suggestibility studies found that patients with an FND
exhibited greater suggestibility than controls, SMD=0.48 [0.15, 0.81], Z=2.84, p=.004 (see Figure 2).
Positive results were observed in 8 studies with a high inconsistency of effect sizes across studies, I2=73%.
Jackknife analysis in which each study effect was sequentially omitted and the analysis re-performed
indicated that the group difference was reliably significant (SMD range: 0.40-0.56).
Meta-analysis of 11 symptom suggestibility studies found that patients with FND displayed greater
responsiveness than controls, SMD=1.39 [0.92, 1.86], z=5.77, p<.001 (see Figure 2). Overall positive
responses were observed in 49% of patients with FND and 6% of controls (sensitivity=49%,
specificity=94%). Ten of the 11 studies exhibited positive SMDs although there was substantial
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(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
inconsistency in effect sizes across studies, I2=99%. Jackknife analysis revealed that the group difference
remained significant after omitting each study in a sequential manner (SMD range: 1.25 to 1.54).
The weighted effect size for symptom studies was significantly greater than that for standardized studies,
z=2.60, p=.009. This difference remained stable, z=2.29, p=.022, after removing the two studies included in
both data sets. When the two data sets were aggregated, the cumulative standardised effect size was slightly
Publication bias
Egger’s test did not suggest asymmetry in the distribution of effect sizes in the standardized studies, z=0.69,
p=.49, or in the symptom studies, z=1.50, p=.13. A trim and fill estimate produced only a slight reduction in
effect sizes for standardized studies, ΔSMD=-.05, and symptom studies, ΔSMD=-.10 (see Figure 3).
Given the observed inconsistency in the magnitude of effects, a set of meta-regression analyses considered
whether group differences were moderated by binary and continuous predictors pertaining to study
methodologies (see Table 3). Effect sizes were significantly larger when a hypnotic induction was included
in standardized studies, but not in symptom studies. Effect sizes were also larger in studies that reported
whether suggested symptoms were typical for the patient relative to those that did not report this
information; this implies that effect sizes are not inflated by the inclusion of atypical symptoms in response
rates for suggestive symptom induction. By contrast, effect sizes were not significantly related to the type of
control (clinical vs. non-clinical; standardized studies) or suggestive induction protocol (suggestion vs.
nocebo [suggestion and sham]; symptom studies). Experimenter blindness did not significantly moderate
group differences with numerical differences in opposing directions for standardized and symptom studies.
Similarly, methodological quality related to effect sizes in opposing directions: greater quality was
significantly associated with lower effect sizes in standardized studies, but with larger (albeit non-
significantly) effect sizes in symptom studies. These effects were primarily driven by procedure description.
Standardized effect sizes were smaller in studies that met criteria for clarity of inclusion/exclusion criteria:
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z=-2.54, p=.011; diagnostic procedure: z=-2.82, p=.005; and scale administration procedure: z=-2.28, p=.022
(all other ps>.09). In contrast, symptom effect sizes were larger in studies that met criteria for clarity of
Discussion
The results of this meta-analysis suggest that FND patients display elevated suggestibility on standardized
behavioural scales and in response to suggestive symptom induction protocols, consistent with theoretical
predictions to this effect.7, 20, 21 There was no evidence for publication bias although there was considerable
heterogeneity in both data sets, which was partly explained by methodological variability.
These findings are consistent with models proposing responsiveness to suggestion as a vulnerability
factor for FND and those attributing functional symptoms to precise symptom priors.8, 13 Recent theoretical
work conceptualizes functional symptoms as arising from an interaction between multiple factors including
an autonomic arousal response, inhibitory deficits that increase the likelihood of body misrepresentation,
and symptom priors that collectively trigger the automatic activation of rogue symptom representations or
dissociative responses to stressors. Moreover, suggestibility has been proposed to reflect a generalized
tendency to form precise priors that override various motor and perceptual systems,31 which is thought to be
a key process in FND13 and symptom reporting more generally.14 This aligns with research showing that
hypnotic suggestibility predicts symptom severity in FND patients.32 Observed links between hypnotic
suggestibility and emotional responsiveness to social cues,23 highlight the potential role of suggestibility in
symptom modeling or triggering through social observation.8 The perception that functional symptoms are
Although the two forms of suggestibility moderately covary,33 FND patients were more responsive to
symptom-specific (SMD=1.39 [0.92, 1.86]) than to standardized suggestions (SMD=0.48 [0.15, 0.81]),
implying selectively greater suggestibility for functional symptoms. Indeed, the sole non-significant
provocation study34 administered suggestions for generic symptoms that did not necessarily mirror patients’
symptom profiles. Previous research similarly found that highly dissociative individuals and dissociative and
acute stress disorder patients are more responsive to suggestions for dissociative experiences (e.g.,
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
amnesia).19 Symptom suggestibility in FND may thus partly reflect a kindling process whereby symptoms
Atypical suggestibility in FND patients complements research showing greater suggestibility in germane
conditions, such as dissociative and stress disorders19, 20 and somatoform disorders.35 Many of these
symptoms may account for heterogeneity in the suggestibility profiles of FND patients, with heightened
responsiveness to suggestions being specific to, or more pronounced among, patients with marked
induction was associated with greater standardized suggestibility among FND patients. This is consistent
with the proposal that individuals with compartmentalization symptoms benefit more from a hypnotic
These effects attest to the efficacy of suggestion in the diagnosis of FND.15 Suggestive symptom
induction displayed high specificity (94%) although sensitivity is poor (49%), indicating that this technique
is insufficient as a standalone diagnostic procedure. The inclusion of sham methods or a hypnotic induction
were not associated with greater discrimination of FND patients and controls relative to verbal suggestion
alone but warrant further attention. Suggestive symptom induction is likely to be especially valuable in
suggestible populations such as adolescent and elderly samples23 or patients with comorbid dissociative or
stress disorder diagnoses.19, 20 It may also inform diagnosis of comorbid non-epileptic seizures in epilepsy
patients38 and medication prescription in FND patients.39 Insofar as suggestibility is a positive predictor of
outcome with suggestion-based treatments,18 these results also support greater incorporation of suggestion
techniques in treatment protocols, which show promising results in randomized-controlled trials.16 However,
they also highlight the need to control for suggestion, or consider its role, in diagnostic and treatment
Limitations
The principal limitations of these data concern methodological variability across studies. Methodological
quality was significantly or descriptively related to effect sizes in both data sets albeit in opposite directions.
Among standardized studies, older studies that did not precisely specify inclusion/exclusion criteria and/or
diagnostic and scale administration procedures tended to exhibit larger effect sizes; in contrast, precise
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
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specification of diagnostic procedures was associated with larger effect sizes in symptom studies. In most
studies, the operator administering the assessment was not blind to patient group, which may inflate effect
sizes22, although there was no evidence for an experimenter effect in the standardized studies. The sole blind
symptom study had a lower effect size than the remainder of the studies but was still large in magnitude
(SMD=0.93 [0.61, 1.26]). Most studies included clinical controls (e.g., epilepsy patients), which raises issues
regarding generalizability although effect sizes did not significantly relate to control type. Symptom
suggestibility estimates are also confounded by baseline symptom frequency, which is not incorporated into
these assessments.15 This potentially renders patients with high symptom frequency at an increased risk of
false positive responses, although there is evidence that this is not the case.40 The studies also varied in
whether successful responses to symptom induction protocols were contingent upon the typicality of the
response, which accounted for variability in effect sizes. Standardized studies were limited insofar as only
one controlled for compliance. In addition, standardized suggestibility scales include a disproportionate
number of suggestions for dissociative and functional symptoms (e.g., paralysis),20, 23, 32 raising the question
of whether elevated suggestibility in FND generalizes beyond these symptoms. Collectively, these findings
underscore the need for optimization and standardization of suggestive symptom induction protocols,15
Conclusions
This meta-analysis corroborates the long-held view that FND is characterized by elevated suggestibility.
Increased suggestibility has direct implications for the risk factors underlying this condition, the use of
suggestion to aid diagnosis, the utility of suggestion-based treatments for functional symptoms, and
Acknowledgements
The authors thank Che Ofuasia, Goldsmiths, University of London, for contributing to the data coding and
evaluation.
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
Contributors
All authors conceived the project. LW carried out the database searches and data coding with assistance
from RJB, TT, and DBT. LW and DBT performed the meta-analysis with assistance from RJB and TT. LW
and DBT drafted the initial manuscript. All authors reviewed and approved the final version of the
manuscript.
Funding
This study was supported by Bial Foundation bursary 70/16 (DBT) and a Gyllenbergs Foundation
fellowship (DBT).
Competing interests
Not required.
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Figure 2. Forest plots of Standardised Mean Differences (SMDs) (with 95% confidence intervals) from
(left) 11 standardized suggestibility studies and (right) 11 symptom suggestibility studies. Marker sizes
Figure 3. Funnel plots of standardized mean differences (SMDs) from (left) 11 standardised suggestibility
studies and (right) 11 symptom suggestibility studies. Filled circles denote individual study effect sizes and
empty circles denote estimated missing individual effect sizes due to publication bias imputed using the trim
and fill method. Summary SMDs [95% CI] using the trim-and-fill method were SMD=0.43 [0.10, 0.76]
(standardized suggestibility studies) and SMD=1.29 [0.84, 1.75] (symptom suggestibility studies).
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
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1991*
Barry et al., 2000 - MI, CR NES/ES 36 (-) - (-) ES 22 (-) - (-) HIP Y
Goldstein et al., - MI, CR NES 20 (80) 34.4 (12.4) NCC 20 (45) 36 (8.5) CIS N
2000
Kuyk et al., 1999 - MI NES 20 (80) 25 (-) ES 17 (18) 37 (-) SHCS Y
Kuyk et al., 1995 - MI, CR NES 6 (50) 19.3 ES 7 (14) 28.6 (-) SHCS Y
Formal Procedure Diagnosis n (% Age Diagnosis n (% Age Suggestion/noceb Hypnotic FND Control
female) [M (SD)] female) [M (SD)] o induction
Kandler et al., - MI, CR NES 416 (-) - (-) ES 568 (-) - (-) VS, HV, PS N 120 40 (7%)
2018 (29%)
Chen-Block et al., - MI, CR NES/ES 466 - (-) ES 581 - (-) VS, HV, PS, AP, N 240 15 (3%)
2016 (70) (54) ST (52%)
Goyal et al., 2014 - MI NES 140 21.38 ES 50 (34) 21.18 VS, PS, VTF, N 84 (60%) 0 (0%)
(71) (10.83) (9.98) TC, MS, SI
Arain et al., 2009 - MI NES 24 (67) - (-) ES 54 (65) - (-) VS, HV N 8 (33%) 6 (11%)
Khan et al., 2009 - MI NES 24 (-) - (-) ES 16 (-) - (-) VS Y 11 (46%) 2 (13%)
Kenney et al., FW PDF PT 12 (-) 42.5 (11) ET 33 (-) 56.8 (17) VS, HV, VTF N 6 (50%) 5 (15%)
2007
Martinez-Taboas, - CR, PDF NES 8 (88) 32 (9.2) ES 5 (100) 30 (6.2) VS, ARS Y 8 (100%) 0 (0%)
2002
Barry et al., 2000 - MI, CR NES/ES 47 (-) - (-) ES 22 (-) - (-) VS Y 36 (77%) 1 (5%)
Chabrol et al, DSM- CR, PDF CD 15 (-) 44 (14) mND 40 (-) 53 (17) VS N 6 (40%) 17 (43%)
1995 IV
Lancman et al., - MI NES 93 (77) 26.7 (-) ES 20 (70) 28.2 (-) VS, AP N 72 (77%) 0 (0%)
1994
Walczak et al., MI NES 40 (90) 33.9 (11.6) ES 20 (45) 34 (11.7) VS, SI N 33 (83%) 5 (25%)
1994
Notes. DSM=Diagnostic and Statistical Manual of Mental Disorders (American Psychiatric Association); MI=Medical
investigations; CR=case note review for ruling out organic causes; PDF=positive diagnostic features; Fahn and Williams diagnostic
criteria; NES=non-epileptic seizures; ES=epileptic seizures; PT=psychogenic tremor; CD=conversion disorder; ES=essential tremor;
mND=mixed neurological disorders; VS = verbal suggestion; HV=hyperventilation; PS=photic stimulation; AP=alcohol patch;
ST=subjective trigger; VTF=vibrating tuning fork; TC=temple compression; MS=moist swab; SI=saline injection; ARS=age
regression suggestion; - = Not reported.
medRxiv preprint doi: https://doi.org/10.1101/2020.05.30.20117705; this version posted June 3, 2020. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
Table 3. Meta-regression analyses for standardized and symptom suggestibility studies (SMD [95% CIs] (k))
Moderator
Suggestibility type Analysis groups Z p I2