Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
Healthy Volunteers
ID06980090

Neural Mechanisms of Interpersonal Expectations on Negative Affect Using Transcranial Temporal Interference Stimulation

Led by Trustees of Dartmouth College · Updated on 2026-04-24

190

Participants Needed

1

Research Sites

26 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are studying whether a non-invasive brain stimulation method called transcranial temporal interference stimulation (tTIS) can reduce negative feelings, and how expectations shaped by care providers affect these results. The study aims to find out if active tTIS works better than sham (inactive) tTIS, and if positive treatment expectations improve the effects compared to negative ones. This research involves healthy adults aged 18 to 55 and uses a randomized, triple-blind design to explore these questions. The study has two experiments with different designs. Experiment 1 involves 30 participants who each complete four sessions combining active or sham tTIS with positive or negative placebo messaging. Active tTIS delivers specific electrical signals targeting the brain for 20 minutes, while sham tTIS mimics the procedure without effective stimulation. Experiment 2 includes 160 participants divided into patients and doctors; patients undergo two sessions with sham tTIS paired with either a social placebo intervention or no intervention, while doctors are trained to provide placebo messaging and monitor patient responses. Sessions are spaced at least 48 hours apart. Participants complete tasks that assess negative affect before and after each session, including cognitive effort, fear, and pain ratings. Physiological data such as heart rate, skin conductance, and others are recorded during the sessions. Additional assessments include MRI scans and behavioral measures. The study tracks changes in negative affect and physiological responses over approximately one month, with safety and tolerability monitored throughout.

CONDITIONS

Brief Title

Neural Mechanisms of Interpersonal Expectations on Negative Affect

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 55 years
  • Medical students or resident physicians may participate as 'doctors'
  • Participants able to perform experimental tasks and fluent or native English speakers
  • Participants must tolerate the maximum level of thermal pain stimuli used in the study
  • Participants without current or history of psychiatric or neurological conditions as specified
Not Eligible

You will not qualify if you...

  • Current or history of depression, bipolar disorder, or other psychiatric diagnosis
  • Current seizure disorder or history of stroke or major neurological diagnosis causing cognitive impairment
  • Current chronic pain or acute pain within three months of the study
  • Current migraine disorder with 15 or more headache days in one month
  • Use of central nervous system-effective medication or other neurological/psychiatric treatments
  • Substance abuse within the last six months
  • Contraindications to MRI or tTIS (including pregnancy, claustrophobia, pacemakers, implants, shrapnel, brain abnormalities, scalp lesions)
  • Contraindications for induced pain (including heart disease, high blood pressure, heart surgery, severe asthma, respiratory problems, fibromyalgia, Raynaud's Syndrome, diabetes)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Experiment 1 Treatment Sessions

Duration - At least 8 days (4 sessions with minimum 48 hours between each)

Participants complete four experimental sessions involving different combinations of active or sham transcranial temporal interference stimulation (tTIS) paired with positive or negative social placebo interventions. Each session includes completing multimodal negative affect tasks before and after stimulation.

4 sessions (in-person) with at least 48 hours between each

Experiment 2 Treatment Sessions

Duration - At least 2 days (2 sessions with minimum 48 hours between each)

Participants complete two experimental sessions involving sham tTIS paired with either a positive social placebo intervention or no placebo intervention. Each session includes completing multimodal negative affect tasks before and after stimulation, along with MRI scanning and physiological monitoring.

2 sessions (in-person) with at least 48 hours between each

Trial Site Locations

Total: 1 location

1

Dartmouth College, Department of Psychological and Brain Sciences

Hanover, New Hampshire, United States, 03755

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Research Team

Z

Zhaoxing Wei, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

6

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Published Research Related To This Trial

Noninvasive theta-burst stimulation of the human striatum enhances striatal activity and motor skill learning.

Maximilian J Wessel, Elena Beanato, Traian Popa...

https://pubmed.ncbi.nlm.nih.gov/37857774