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Effects of External Ear Stimulation on Pain Perception and Mood

Effects of External Ear Stimulation on Pain Perception and Mood

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02821741
Enrollment
76
Registered
2016-07-04
Start date
2016-10-18
Completion date
2027-03-30
Last updated
2026-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain in Healthy Participants

Keywords

Sensory Stimulation

Brief summary

Background: The vagus nerve runs from the brain to many organs. Stimulating it can affect the experience of pain. The nerve can be stimulated on the surface of the left ear. Researchers want to study how this stimulation affects the perception of pain. They also want to study how mood affects the experience of pain. Objective: To study the effects of mood and vagus nerve stimulation on the experience of pain. Eligibility: Healthy people ages 18 and older who are fluent in English Design: Participants will be pre-screened with a 15-minute phone call. Participants will have three 2-hour visits. At the screening visit, participants will be screened with: Medical and psychiatric history Physical and psychological exams Questionnaires about physical and psychiatric health and mood Urine tests A heat probe on the forearm. The temperature will be increased until it is painful but tolerable. Participants will have 2 testing sessions within 7 days. Before the testing, they cannot do the following: Eat, use nicotine, or exercise for at least 2 hours Drink alcohol for 24 hours Take certain medicines for 3 days Testing includes: Urine drug screening Left ear stimulation: In one session, the vagus nerve will be stimulated. In the other, an area of the ear away from the vagus nerve will be stimulated. This will be done with mild electric shocks that cause a tingling, pricking, or itchy feeling. Heat applied to the forearm until it is painful but tolerable Completing several forms on a computer or on paper about how they are feeling Monitors on the chest and a finger clip to monitor heart, breathing, and blood pressure

Detailed description

This double-blind, randomized, controlled, cross-over study on healthy participants will evaluate the perceptual differences of pain and changes in mood in response to peripheral nerve stimulation over two regions of the left external ear. A series of short and long duration heat stimuli will be applied to the participants forearms and they will be asked to rate their current mood state, the intensity of the pain, and whether it was pleasant or unpleasant. The series of heat stimuli will be applied before, during, and after mild electrical stimulation of the left external ear using a commercially available TENS unit. There are two study sessions. Session 1 involves eligibility screening, a brief practice session, followed by the testing session. In Session 2 (no more than 7 days later), the testing session will be repeated with the exception of the location of ear stimulation. Up to 76 people, ages 18-50 years old, will be enrolled in the study.

Interventions

DEVICEThe Twin Stim Plus, 3rd Edition

Mild transcutaneous electrical stimulation will be applied to the cymba conchae of the left ear on day 1 and the left earlobe on day 2 (or vice versa) using a commercially available TENS unit (transcutaneous electrical nerve stimulator) attached to a pair of silver electrodes.

DEVICEMedoc Pathway System

Device used to apply Thermal stimulation to both arms.

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* INCLUSION CRITERIA: All subjects must be: 1. between 18 and 50 years old. 2. fluent in English. 3. able to provide written informed consent.

Exclusion criteria

Overall

Design outcomes

Primary

MeasureTime frameDescription
The difference in pain ratings collected for each subject during the two types of left ear stimulation (cymba conchae and earlobe).End of studySee measures

Secondary

MeasureTime frameDescription
The effect of tVNS on pain threshold, pain unpleasantness, and mood as measured by visual analogue scales (VAS).End of StudySee measures
Mood and anxiety, as measured by questionnaires taken at the beginning and end of both study sessions.End of studySee measures
Autonomic measures will be analyzed to determine whether tVNS has an effect on heart rate variability.End of studySee measures

Countries

United States

Contacts

CONTACTHayley A Owens
hayley.owens@nih.gov(301) 451-2413
CONTACTAlisa J Johnson
alisa.johnson@nih.gov(240) 603-0537
PRINCIPAL_INVESTIGATORAlisa J Johnson

National Center for Complementary and Integrative Health (NCCIH)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026