Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
Healthy Volunteers
NCT06986122

Virtual Contexts for Affective Modulation

Led by Trustees of Dartmouth College · Updated on 2025-10-31

20

Participants Needed

1

Research Sites

189 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study investigates how spatial context and perceived controllability modulate pain, affective states such as anxiety, and motivated behavior. The study examines how control over pain and threat-related environments influences pain perception, state anxiety, associated autonomic responses, and behavior. The main questions it aims to answer are: Does having control over pain within specific contexts alter how much pain people feel-even when the stimulus intensity remains constant? How do different types of environments (safe, controllable, or uncontrollable) shape pain-related brain activity, subjective anxiety, and physiological arousal? How do people perform cognitively demanding or distracting tasks (and retain their memory) when under threat versus when in control? Lastly, how do these learned associations with spatial contexts persist or adapt when environmental contingencies are explicitly changed? Taken together, exploration of these factors may lay the groundwork for understanding how placebo-related mechanisms-including perceived control, contextual learning, emotional engagement, and distraction-interact to shape pain and anxiety in complex environments.

CONDITIONS

Official Title

Virtual Contexts for Affective Modulation

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 55 years
  • Fluent or native English speakers
  • Able to perform study tasks such as reading and navigating virtual environments
  • Able to tolerate the maximum level of thermal pain stimuli used in the study
Not Eligible

You will not qualify if you...

  • Current or past diagnosis of depression, bipolar disorder, or other psychiatric conditions
  • Current seizure disorder within past 10 years, history of stroke, or major neurological diagnosis
  • Current chronic pain or acute pain within the last 3 months
  • Current migraine disorder with 15 or more headache days in one month
  • Use of central nervous system medications or other neurological/psychiatric treatments
  • Substance abuse within the last 6 months
  • Contraindications to MRI such as pregnancy, claustrophobia, pacemakers, implants, shrapnel, brain abnormalities, or 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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Trial Site Locations

Total: 1 location

1

Dartmouth College

Hanover, New Hampshire, United States, 03755

Actively Recruiting

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Research Team

T

Tor D Wager, PhD

CONTACT

V

Vivek Sagar, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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