Reduce High-risk Behaviours Under Chronic Stress Via tDCS-induced Neural Plasticity

Sponsor
LI Cheng (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05501951
Collaborator
(none)
255
3
20

Study Details

Study Description

Brief Summary

The persistent political conflicts and COVID-19 pandemic have led to elevated chronic stress levels in Hong Kong, with far-reaching and profound negative impacts on the citizen's mental health. An important pathway via which chronic stress negatively impacts health is through promoting high-risk behaviours, such as addiction, suicide, and antisocial acts. Therefore, testing means to break the association between chronic stress and high-risk behaviour is essential to reducing the adverse consequences of stress and promoting stress resilience. The transcranial direct current stimulation (tDCS) may be a viable method for reducing risky tendency in high-stress individuals, through modulating brain functions and plasticity. Although single-session tDCS has been shown to reliably reduce risky decision making and behaviours acutely, its efficacy over extended periods of time has not been demonstrated, particularly among non-clinical samples. Being able to show that tDCS could lead to long-lasting reduction of risky tendency is necessary for promoting the wide application of this method in therapeutic settings. In this project, we aim to conduct a randomised control trial to systematically and comprehensively test whether 10 sessions of tDCS on either the dorsolateral prefrontal cortex or the orbitofrontal cortex would lead to reduction in risky tendency not only immediately after treatment, but also at 1 month and 3 months after treatment.

Participants will be healthy male and female adults (21-40 years old) under relatively high levels of chronic stress, as selected from an online survey prior to the study.

Participants will be randomly allocated to one of 3 treatment groups: DLPFC tDCS, OFC tDCS, and sham control. At baseline, participants will complete several risk-taking assessments, including an established computerised task that measures both risk taking and a cognitive bias that was shown to increase irrational risky tendency (illusion of control), an established questionnaire that measures risky decision making in real-life scenarios, and a scale measuring past engagement in common risky activities.

Participants will also complete various personality and mood questionnaires, along with assessments on important cognitive abilities. We hypothesized that both DLPFC and OFC tDCS would reduce risk taking across the 3 timepoints, but the effect of DLPFC tDCS would be mediated by reduction in cognitive bias, whereas that of OFC tDCS would be mediated by increase in inhibition functions. These hypotheses will be tested by linear mixed models and mediation analyses. Additional exploratory analyses also test whether the tDCS effect would be moderated by relevant personality factors such as impulsivity.

Condition or Disease Intervention/Treatment Phase
  • Other: tDCS stimulation
  • Other: Sham stimulation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
255 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Reduce High-risk Behaviours Under Chronic Stress Via tDCS-induced Neural Plasticity
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: right DLPFC tDCS

Participants in this group will receive 10 sessions of right DLPFC tDCS

Other: tDCS stimulation
The transcranial direct current stimulation (tDCS) method has emerged in the recent years as a non-invasive, safe, cheap, convenient and effective means to modulate brain functions and behaviours

Experimental: right OFC tDCS

Participants in this group will receive 10 sessions of right OFC tDCS

Other: tDCS stimulation
The transcranial direct current stimulation (tDCS) method has emerged in the recent years as a non-invasive, safe, cheap, convenient and effective means to modulate brain functions and behaviours

Sham Comparator: Control group

Participants in this group will receive 10 sessions of sham stimulation

Other: Sham stimulation
For the sham group, the electrode positioning will be randomly allocated to be identical to either the DLPFC or the OFC group, and active stimulation will be delivered for the first 30 seconds only

Outcome Measures

Primary Outcome Measures

  1. Changes in risk taking behavior [Baseline; 1-month follow up; 3-month follow up]

    Changes in risk taking will be assessed using the IoC card gambling task

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged between 21-40 years;

  • Fluent in reading and writing Chinese (Cantonese or Mandarin);

  • Right-handed as assessed with the Edinburgh Handedness Inventory;

  • Normal or corrected-to-normal vision and hearing;

  • IQ>90 as assessed with the Test of Nonverbal Intelligence, 4th edition (TONI-IV)

Exclusion Criteria:
  • Past or present physical illness, organic brain disorder, traumatic brain injury, addiction, impulse control disorder, psychotic disorder, affective disorder, or any other major neurological or psychological condition;

  • First-degree relative with past or present major psychological disorder or suicidal behaviour;

  • Intake of psychotropic medication or any other medication that may affect cognition in the 6 months preceding the study day;

  • (For women) being pregnant;

  • any contraindication for tDCS, such as having a cerebral implant or history (either personal or family) of seizure. The psychological conditions will be assessed using the Structured Clinical Interview for DSM-5 Disorders-Clinician Version (SCID-5-CV).

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • LI Cheng

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
LI Cheng, Postdoctoral fellow, The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05501951
Other Study ID Numbers:
  • tDCSHKU
First Posted:
Aug 16, 2022
Last Update Posted:
Aug 16, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 16, 2022