tDCS in Treatment of Craving in Sexual Addiction (CAS)
Primary Purpose
Sexual Addiction, Hypersexualism
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Active Trans-cranial direct current stimulation (tDCS)
Sham Trans-cranial direct current stimulation (tDCS)
Sponsored by
About this trial
This is an interventional treatment trial for Sexual Addiction focused on measuring Sexual Addiction, Hypersexualism, Neurostimulation, tDCS, fMRI
Eligibility Criteria
Inclusion Criteria:
- 18-60 year old male
- Heterosexual
- Right-handed (Manual laterality test)
- With a sexual addiction (PEACCE Tool> 3 and Carnes ≥ 13/25) except for controls
- Having signed a written and informed consent
- Subject benefiting from social security
Exclusion Criteria:
- Subject presenting a medical pathology requiring drug treatment,
- Severe psychiatric pathology (bipolar disorder, hyperactivity or schizophrenia) or another addiction (alcohol, illicit substances or behavioral addiction)
- Subject consuming psychotropic drugs in progress or during the last month
- Subject not understanding French
- Subject under tutorship or curatorship
- Subjects with neurological disease including epilepsy or a history of head trauma
- Subjects hospitalized in enforced hospitalization
- Subject presenting a contraindication to tDCS: subject with an electrical or metal brain implant
- Subject with a contraindication to MRI
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Patient with sexual addiction - active stimulation
Patient with sexual addiction - sham stimulation (placebo)
Arm Description
25 patients with sexual addiction will be stimulated by active tDCS during 5 consecutive days
25 patients with sexual addiction will be stimulated by sham tDCS stimulation (placebo) during 5 consecutive days
Outcomes
Primary Outcome Measures
Efficacy of tDCS in treatment of craving of sexual addiction
The primary outcome is to assess the effectiveness of tDCS treatment on the reduction of the craving by comparing before and after active tDCS stimulation in response to erotic-pornographic images.
Efficacy will be quantified by a sexual craving scale associated with erotico-pornographic images before and after tDCS stimulation.
A significant decrease in craving and score on the scale is expected after tDCS stimulation. compared to control subjects. Images of social and neutral interactions will be used as comparison of expected changes.
The scale used is the PATHOS scale: brief sexual addiction screening questionnaire.
Efficacy of tDCS in treatment of sexual addiction in subjective emotional response
For the evaluation of efficacy of tDCS in emotional response, indirect measurement of craving, visual emotional responses scales (Likert) will be used during visualization of erotico-pornographic images, before and after stimulation. The "desire" will be quantified on a Likert scale from 0 to 7.
Efficacy of tDCS in treatment of sexual addiction in objective emotional response
An assessment of emotional responses will also be done using heart rate measure during visualization of images in fMRI, before and after stimulation by tDCS
Secondary Outcome Measures
Brain structures involved in sexual addiction
The secondary objectives are the evaluation of the brain structures involved in sexual addiction, especially craving, and the study of the modifications of the circuits involved after the application of tDCS.
A modification of the BOLD signal in fMRI in the mesolimbic reward system as well as in the dorsolateral prefrontal cortex, orbitofrontal cortex and the amygdala in response to erotic images is expected after tDCS. 50 patients with sexual addiction will be compared with 25 healthy subjects for this objective
Evaluation of Impulsivity with The Barratt Impulsiveness Scale
In addition, the evaluation of impulsivity and inhibition capacities of the frontal cortex will be conducted.Changes in impulsivity scale scores and motor inhibition task scores are expected after tDCS.
Evaluation of Impulsivity with UPPS-P Impulsive Behavior Scale
A decrease in scores on this scale is expected after stimulation compared to patients who received placebo stimulation.
Evaluation Evaluation of Impulsivity with Stop Signal Task
A decrease in scores on this scale is expected after stimulation, compared to patients who received placebo stimulation.
Full Information
NCT ID
NCT04923451
First Posted
March 22, 2021
Last Updated
June 9, 2021
Sponsor
Centre Hospitalier St Anne
1. Study Identification
Unique Protocol Identification Number
NCT04923451
Brief Title
tDCS in Treatment of Craving in Sexual Addiction
Acronym
CAS
Official Title
Transcranial Electrical Stimulation in Sexual Addiction: an Innovative Treatment for a Better Understanding of the Physiopathology of Craving
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 1, 2021 (Anticipated)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
October 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier St Anne
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In patients with addiction to a substance, an increase in activity in the prefrontal cortex induced by transcranial Direct Current Stimulation -tDCS (non-invasive technique, modulating cortical activity by applying low-intensity electrical currents between two electrodes),may help reduce craving in people addicted to alcohol and tobacco. By analogy with addictive behavior with a substance, the craving observed in certain behavioral addictions would involve the same neural circuits.
The main hypothesis is to reduce the sexual craving associated with the viewing of erotic images during active brain stimulation compared to placebo stimulation. Functional MRI will allow to better understand the neural circuits involved in sexual addiction and in the expected inhibition of sexual arousal by tDCS in sexual addictions during visualization erotic images.
Detailed Description
The concept of sexual addiction appeared in American literature about 20 years ago. The term sexual addiction describes an excessive, increasing, and especially uncontrolled frequency of sexual behavior, as a conventional rule, associated with a compelling and irrepressible sexual desire (craving), which persists in spite of the possible negative consequences and personal suffering of the subject. The prevalence of this condition is estimated to be approximately 3-6% in the general population in the United States, it is independent of the socio-cultural environment. The pathophysiology of sexual addictions remains very poorly understood.
Numerous studies have focused on substance addictions and their pathophysiology. The mesolimbic dopaminergic system plays a major role in addictive behavior. The prefrontal cortex and the basolateral region of the amygdala play an important role in the craving and may cause relapse in subjects. In subjects with sexual addiction, only one controlled study has been conducted on the role of antidepressant treatment in the reduction of craving. The objective of the study is not only to evaluate the efficacy of tDCS neurostimulation in this disorder but also to identify the brain structures involved in this addictive disorder.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sexual Addiction, Hypersexualism
Keywords
Sexual Addiction, Hypersexualism, Neurostimulation, tDCS, fMRI
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Quantitative data regarding the intensity of emotional response and craving to erotic images, motor inhibition task and impulsivity will be presented in the form of frequency, mean and standard deviation (SD) calculations and compared using a 2-factor repeated measures ANOVA taking into account the fact that the patient will be compared to himself (position 1 and 2 and placebo) and to other patients using 3 kinds of images (erotic, social and neutral) with 3 types of possible stimulations.
In order to analyze the fMRI data, the regions of the patient's body will be identified. in which the BOLD activity will be correlated to the attractiveness of the image. Foreach patient, the difference before and after stimulation will be calculated. There will be no intermediate analysis.
Masking
ParticipantCare Provider
Masking Description
Depending on the randomized group, the subject will receive one of two treatments 15 days apart (A: active anode on the right DLPFC and neutral cathode on the left shoulder; B: inactive anode on the DLPFC and inactive cathode on the left shoulder). The groups are defined as follows:
The results of randomization will not be known by the evaluator.
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Patient with sexual addiction - active stimulation
Arm Type
Active Comparator
Arm Description
25 patients with sexual addiction will be stimulated by active tDCS during 5 consecutive days
Arm Title
Patient with sexual addiction - sham stimulation (placebo)
Arm Type
Sham Comparator
Arm Description
25 patients with sexual addiction will be stimulated by sham tDCS stimulation (placebo) during 5 consecutive days
Intervention Type
Device
Intervention Name(s)
Active Trans-cranial direct current stimulation (tDCS)
Intervention Description
5 active sessions (1/day for 5 consecutive days) of tDCS (NeuroConn DC), active anode 8cm2 on right dorso-lateral prefrontal cortex and neutral cathode, 2 mA, during 30 min will be performed
Intervention Type
Device
Intervention Name(s)
Sham Trans-cranial direct current stimulation (tDCS)
Intervention Description
5 placebo sessions (1/day for 5 consecutive days) of sham tDCS (NeuroConn DC), anode 8cm2 on right dorso-lateral prefrontal cortex and neutral cathode during 30min will be performed
Primary Outcome Measure Information:
Title
Efficacy of tDCS in treatment of craving of sexual addiction
Description
The primary outcome is to assess the effectiveness of tDCS treatment on the reduction of the craving by comparing before and after active tDCS stimulation in response to erotic-pornographic images.
Efficacy will be quantified by a sexual craving scale associated with erotico-pornographic images before and after tDCS stimulation.
A significant decrease in craving and score on the scale is expected after tDCS stimulation. compared to control subjects. Images of social and neutral interactions will be used as comparison of expected changes.
The scale used is the PATHOS scale: brief sexual addiction screening questionnaire.
Time Frame
3 years
Title
Efficacy of tDCS in treatment of sexual addiction in subjective emotional response
Description
For the evaluation of efficacy of tDCS in emotional response, indirect measurement of craving, visual emotional responses scales (Likert) will be used during visualization of erotico-pornographic images, before and after stimulation. The "desire" will be quantified on a Likert scale from 0 to 7.
Time Frame
3 years
Title
Efficacy of tDCS in treatment of sexual addiction in objective emotional response
Description
An assessment of emotional responses will also be done using heart rate measure during visualization of images in fMRI, before and after stimulation by tDCS
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Brain structures involved in sexual addiction
Description
The secondary objectives are the evaluation of the brain structures involved in sexual addiction, especially craving, and the study of the modifications of the circuits involved after the application of tDCS.
A modification of the BOLD signal in fMRI in the mesolimbic reward system as well as in the dorsolateral prefrontal cortex, orbitofrontal cortex and the amygdala in response to erotic images is expected after tDCS. 50 patients with sexual addiction will be compared with 25 healthy subjects for this objective
Time Frame
3 years
Title
Evaluation of Impulsivity with The Barratt Impulsiveness Scale
Description
In addition, the evaluation of impulsivity and inhibition capacities of the frontal cortex will be conducted.Changes in impulsivity scale scores and motor inhibition task scores are expected after tDCS.
Time Frame
3 years
Title
Evaluation of Impulsivity with UPPS-P Impulsive Behavior Scale
Description
A decrease in scores on this scale is expected after stimulation compared to patients who received placebo stimulation.
Time Frame
3 years
Title
Evaluation Evaluation of Impulsivity with Stop Signal Task
Description
A decrease in scores on this scale is expected after stimulation, compared to patients who received placebo stimulation.
Time Frame
3 years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18-60 year old male
Heterosexual
Right-handed (Manual laterality test)
With a sexual addiction (PEACCE Tool> 3 and Carnes ≥ 13/25) except for controls
Having signed a written and informed consent
Subject benefiting from social security
Exclusion Criteria:
Subject presenting a medical pathology requiring drug treatment,
Severe psychiatric pathology (bipolar disorder, hyperactivity or schizophrenia) or another addiction (alcohol, illicit substances or behavioral addiction)
Subject consuming psychotropic drugs in progress or during the last month
Subject not understanding French
Subject under tutorship or curatorship
Subjects with neurological disease including epilepsy or a history of head trauma
Subjects hospitalized in enforced hospitalization
Subject presenting a contraindication to tDCS: subject with an electrical or metal brain implant
Subject with a contraindication to MRI
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Leo Malandain, MD
Phone
0033158411678
Email
leo.malandain@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Florence Thibaut, MD-PHD
Email
florence.thibaut@aphp.fr
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
20666699
Citation
Garcia FD, Thibaut F. Sexual addictions. Am J Drug Alcohol Abuse. 2010 Sep;36(5):254-60. doi: 10.3109/00952990.2010.503823.
Results Reference
background
PubMed Identifier
32377953
Citation
Malandain L, Blanc JV, Ferreri F, Thibaut F. Pharmacotherapy of Sexual Addiction. Curr Psychiatry Rep. 2020 May 7;22(6):30. doi: 10.1007/s11920-020-01153-4.
Results Reference
background
PubMed Identifier
17194276
Citation
Wainberg ML, Muench F, Morgenstern J, Hollander E, Irwin TW, Parsons JT, Allen A, O'Leary A. A double-blind study of citalopram versus placebo in the treatment of compulsive sexual behaviors in gay and bisexual men. J Clin Psychiatry. 2006 Dec;67(12):1968-73. doi: 10.4088/jcp.v67n1218.
Results Reference
background
PubMed Identifier
21402948
Citation
Volkow ND, Wang GJ, Fowler JS, Tomasi D, Telang F. Addiction: beyond dopamine reward circuitry. Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15037-42. doi: 10.1073/pnas.1010654108. Epub 2011 Mar 14.
Results Reference
background
PubMed Identifier
25013940
Citation
Voon V, Mole TB, Banca P, Porter L, Morris L, Mitchell S, Lapa TR, Karr J, Harrison NA, Potenza MN, Irvine M. Neural correlates of sexual cue reactivity in individuals with and without compulsive sexual behaviours. PLoS One. 2014 Jul 11;9(7):e102419. doi: 10.1371/journal.pone.0102419. eCollection 2014.
Results Reference
background
PubMed Identifier
23790248
Citation
Rosenberg KP, Carnes P, O'Connor S. Evaluation and treatment of sex addiction. J Sex Marital Ther. 2014;40(2):77-91. doi: 10.1080/0092623X.2012.701268. Epub 2013 Jun 21.
Results Reference
background
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tDCS in Treatment of Craving in Sexual Addiction
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