The present randomized, double blind, placebo-controlled trial aims at evaluating the efficacy of a tDCS treatment in improving the clinical outcome of adolescents with AN and investigate brain mechanisms acting in AN.
The investigators hypothesized that excitatory tDCS over the left PFC and inhibitory tDCS over the right PFC (anode left/cathode right) may aid in altering/resetting inter-hemispheric balance in children and adolescents with AN, reducing their control over eating behaviors and improving the AN psychopathology. Furthermore, the investigators will employ TMS-EEG to directly explore the DLPFC activity of children and adolescent with AN, with specific attention to the differences between hemispheres. Moreover, paired pulse TMS and repetitive TMS protocols will be used to investigate the functional mechanisms within the prefrontal cortex of youth patients with AN. Then, the investigators will assess if potential changes of specific biomarkers, such as those related to the endogenous stress response system functioning, will occur after tDCS treatment and will correlate with clinical improvement.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
80
The tDCS active stimulations will be directed to PFC regions for six weeks delivered for three times a week. tDCS will be delivered by a battery driven, constant current stimulator through a pair of saline-soaked sponge electrodes kept firm by elastic bands. The anode will be placed on the left PFC, F3 position according to the 10-20 international EEG system for electrode placement, while the cathode will be placed on the right PFC, F4 position according to the 10-20 international EEG system for electrode placement. Stimulation intensity will be set at 1 milliampere (mA), the duration of stimulation will be 20 min.
The same electrode placement will be used as in the stimulation conditions (left anodal/right cathodal), but the current will be applied for 30 s and will be ramped down without the participants awareness, and will be held three times a week for six weeks.
Bambino Gesù Hospital and Research Institute
Rome, Italy
RECRUITINGThe primary end-point of the study is the variance on eating psychopathology at T1, assessed as changes in Eating Disorder Risk score (EDRC) of the Eating Disorder Inventory (EDI-3). Significant changes in Ineffectiveness (IC) of the EDI-3.
EDI-3 comprises 91-item that give a measure of the basic characteristics of the ED through six composite scores \[Eating Disorder Risk (EDRC) (range 0-100), Ineffectiveness (IC) (range 0-48), Interpersonal Problems (IPC) (range 0-52), Affective Problems (APC) (range 0-62), Overcontrol (OC) (range 0-52), and General Psychological Maladjustment (GPMC) (range 0-252)\]. Higher scores indicates more severe problems.
Time frame: 6 weeks
Significant changes in Ineffectiveness (IC) of the EDI-3.
Evaluation of the change in Ineffectiveness, with maximum possible score of 48, where higher scores indicate higher Ineffectiveness.
Time frame: 12 months follow up
Significant changes in Interpersonal Problems (IPC) of the EDI-3.
Evaluation of the change in Interpersonal Problems, with maximum possible score of 52, where higher scores indicate higher Interpersonal Problems.
Time frame: 12 months follow up
Significant changes in Affective Problems (APC) of the EDI-3.
Evaluation of the change in Affective Problems, with maximum possible score of 62, where higher scores indicate higher Affective Problems.
Time frame: 12 months follow up
Significant changes in Overcontrol (OC) of the EDI-3.
Evaluation of the change in Overcontrol, with maximum possible score of 52, where higher scores indicate higher Overcontrol.
Time frame: 12 months follow up
Significant changes in General Psychological Maladjustment (GPMC) of the EDI-3.
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Evaluation of the change in General Psychological Maladjustment, with maximum possible score of 252, where higher scores indicate higher General Psychological Maladjustment.
Time frame: 12 months follow up
Significant changes in the total scores of AN symptomatology measures as Eating Attitudes Test (EAT-26)
The EAT-26 proposes a cut-off score of 20. Scores of 20 or higher were considered clinically significant.
Time frame: 12 months follow up
Significant changes in the total scores of AN symptomatology measures as Body Uneasiness Test (BUT).
The BUT proposes a cut-off score of 1,2. Scores of 1,2 or higher were considered clinically significant.
Time frame: 12 months follow up
Significant changes in the total scores of other psychopathological measures as Child Behavior Checklist (CBCL 6-18).
The CBCL 6-18 generates a T-score for each subscale. According to normative data, a T-score above 64 was considered to be significant for the 3 broadband scales, whereas for the syndrome scales, the cut-off for clinical significance was 70.
Time frame: 12 months follow up
Significant changes in the total scores of other psychopathological measures as Children's Depression Inventory (CDI).
Raw scores were converted to T-scores. According to normative data, a T-score above 64 was considered clinical significance.
Time frame: 12 months follow up
Significant changes in the total scores of other psychopathological measures as Multidimensional Anxiety Scale for Children (MASC).
Raw scores were converted to T-scores. According to normative data, a T-score above 64 was considered clinical significance.
Time frame: 12 months follow up
Significant changes in the physiological measures specifically the BMI index
Time frame: 12 months follow up
Number of participants with abnormal laboratory blood test results.
Time frame: 12 months follow up
Significant changes in the endogenous stress response, measured with Cortisol Awakening Response (CAR).
Time frame: 12 months follow up
Significant changes in intra-cortical inhibitory/excitatory motor circuits using paired pulse TMS, measured as short intracortical inhibition and facilitation.
the ratio between MEPs amplitude conditioning stimulus and MEPs amplitude test stimulus alone for each ISI.
Time frame: 6 weeks
Significant changes in sensory-motor integration using paired pulse TMS, measured as SICI/ICF: the ratio between MEPs amplitude (mV) conditioning stimulus (electrical stimulation) and MEP amplitude test stimulus alone for each ISI.
Time frame: 6 weeks
Significant changes in cortical oscillatory patterns (synchronization and desynchronization) in theta, alpha and beta frequencies (Hz) over motor and premotor cortex, using TMS-EEG co-registration.
Time frame: 6 weeks
Significant changes in cortical connectivity using TMS-EEG co-registration combined to report the analysis of the waveform, latency and cortical distribution of TMS-evoked potentials (TEPs) in micronV.
Time frame: 6 weeks
Significant changes in cortical reactivity in terms of TMS-evoked potentials (TEPs) amplitude for time domain (micronV) and frequency bands for spatial domain (Hz), using TMS-EEG co-registration.
Time frame: 6 weeks
Significant changes in Cortical Plasticity evoked by repetitive TMS in terms of different MEP amplitude (mV) recorded at different time-points after repetitive TMS perturbations.
Time frame: 6 weeks