- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05441774
Stimulating Compassion UsingTranscutaneous Vagus Nerve Stimulation
Stimulating Compassion: Using Transcutaneous Vagus Nerve Stimulation (tVNS)
Study Overview
Status
Conditions
Detailed Description
The role of the vagus nerve in regulating cardiac, respiratory, and gut functioning via brainstem nuclei is well-established. More recently, its role has been examined in relation to the modulation of higher cognitive functions. Bodily signals (e.g. from the heart or gut) conveyed by vagal afferents could affect cognitive functioning via projections from the nucleus of the solitary tract (NTS) to the locus coeruleus and thence to widespread cortical areas through noradrenergic outputs. In addition, the NTS transmits sensory-visceral information to the central autonomic network, which includes higher brain areas (e.g. prefrontal cortex). Recent research suggests that vagus nerve activity is associated with a range of psychological functions including memory, executive function, and threat/fear processing. In addition, biobehavioral theories of vagal functioning, and emerging empirical evidence suggest a role for the vagus nerve in modulating social behavior as well as complex emotional states.
A number of researchers have proposed a role for vagal nerve functioning in well-being, and particularly in generating or modulating feelings of 'safeness', contentedness, and relaxation that underlie complex social-affective-motivational states, such as compassion. Previous research has examined the effects of inducing compassionate feelings while measuring vagus nerve activity (via heart rate variability). However, to our knowledge, no published study has demonstrated an association between vagal activity and compassion by directly modulating the vagus nerve itself. Such studies have important theoretical implications but are also potentially valuable in the future development of interventions that employ tVNS or similar technology to augment psychological treatments that employ compassion-focused techniques (e.g. compassionate mind training; compassion-focused cognitive therapy; loving-kindness meditation-based treatments, etc.)
The current experiment aims to determine if vagus nerve activation using tVNS is sufficient to generate positive affective states, especially compassion (specifically, self-reported self-compassion). Alternatively, tVNS may produce a permissive physiological context that facilitates compassionate responding. For example, tVNS may synergize the effects of a compassion-inducing behavioral intervention. To examine these possibilities, the investigators will test the separate and combined (interacting) effects of tVNS and a compassion-induction procedure (self-compassion mental imagery) compared to sham conditions, in a four-group factorial (2 x 2) design. Participants will be randomly assigned to (i) active tVNS + sham imagery, (ii) active tVNS + active self-compassion imagery, (iii) sham-tVNS + active self-compassion and (iv) sham-tVNS + sham imagery.
In addition to examining the effects of stimulation and imagery conditions on self-compassion, the investigators will also test their effects on other types of positive affect, as well as self-criticism, which is an opposing form of self-representation to self-compassion. Self-criticism is a transdiagnostic psychological marker of psychopathology, and measures of self-criticism are sensitive to the effects of compassion-focused interventions , including brief self-compassion imagery, as will be used here. Vagal activity will be indexed using heart rate variability, and effects of stimulation and imagery will additionally be tested on attentional bias (e.g. first fixation, increased dwell time) to compassionate facial expressions.
Participants attend two lab sessions (on Day 1 and 8) in which they will undergo either supervised active or sham tVNS and either the self-compassion or sham imagery exercise (delivered as standardized audio instructions), per their randomized condition. Assessments of heart rate variability, self-compassion, self-criticism, positive state affect, and state mindfulness will occur before stimulation, during stimulation, and after the imagery exercise. In addition, participants will complete the Day 1 stimulation procedure and imagery task on Days 2-7, guided via online audio and written instructions. This will allow us to test the effects of extended (daily) stimulation and imagery practice. Additional study details are available on the Open Science Framework (osf.io/k2dje).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
London, United Kingdom, WC1E 6BT
- Clinical Psychopharmacology Unit
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Fluency in English
- Good (including corrected) vision and hearing.
Exclusion Criteria:
- Current use of any medication for a psychiatric condition
- Regular use of any medication used to treat a cardiovascular condition or inflammation
- Use of any illicit recreational drug >2/week
- Regularly consuming >14 standard UK 'units' of alcohol
- Currently receiving treatment for any mental health condition
- Scores on screening measures of depression (PHQ-2) and/or anxiety (GAD-2) that indicate significant levels of current/recent anxiety or depression (scores on either >4)
- History of serious mental health problems (schizophrenia, bipolar disorder)
- Past or current cardiovascular or neurological problems
- Current/past problems related to chronic/recurring facial or ear pain
- Skin irritation/ broken skin at stimulation site
- Pregnancy or likelihood of becoming pregnant during study
- Previous adverse response to meditation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Sham Comparator: Sham stimulation plus sham imagery
Double sham group: Stimulator electrodes will be applied to earlobe (sham stimulation); imagery task will involve a 'draw-a-face-in-imagination' (sham imagery) task.
|
TVNS is a non-invasive counterpart to surgical methods for stimulating the vagus.
For the sham condition, stimulator electrodes deliver a mild electrical current to the earlobe.
Stimulation parameters: stimulation of left earlobe via two gold-plated electrodes, attached by ear-clip.
Waveform: rectangular, frequency: 20 Hz, pulse width: 0.2 ms, individually adjusted intensity based on participant's perceptual threshold.
Other Names:
Draw-a-face-in-imagination is the sham/ control imagery condition.
Here, control imagery instructions are delivered as a standardized audio-recording, well-matched to self-compassion imagery for number of words, complexity of language, and duration of the audio instructions.
|
|
Other: Active stimulation plus sham imagery
Single (imagery) sham group: Stimulator electrodes will be applied to the tragus (active stimulation); 'draw-a-face-in-imagination' (sham imagery) task.
|
Draw-a-face-in-imagination is the sham/ control imagery condition.
Here, control imagery instructions are delivered as a standardized audio-recording, well-matched to self-compassion imagery for number of words, complexity of language, and duration of the audio instructions.
TVNS is a non-invasive counterpart to surgical methods for stimulating the vagus.
For the active condition, stimulator electrodes deliver a mild electrical current to the tragus.
Stimulation parameters: stimulation of left tragus via two gold-plated electrodes, attached by ear-clip.
Waveform: rectangular, frequency: 20 Hz, pulse width: 0.2 ms, individually adjusted intensity based on participant's perceptual threshold.
Other Names:
|
|
Other: Sham stimulation plus active self-compassion imagery
Single (stimulation) sham group: earlobe (sham) stimulation; imagery task will involve directing compassion to the self (self-compassion, active imagery).
|
TVNS is a non-invasive counterpart to surgical methods for stimulating the vagus.
For the sham condition, stimulator electrodes deliver a mild electrical current to the earlobe.
Stimulation parameters: stimulation of left earlobe via two gold-plated electrodes, attached by ear-clip.
Waveform: rectangular, frequency: 20 Hz, pulse width: 0.2 ms, individually adjusted intensity based on participant's perceptual threshold.
Other Names:
Self-compassion imagery is both a meditative technique and a component of compassion-focused cognitive therapy.
Here, self-compassionate imagery is delivered as standardized audio-recorded instructions.
|
|
Active Comparator: Active stimulation plus active self-compassion imagery
Double active group: tragus (active) stimulation; self-compassion (active imagery)
|
TVNS is a non-invasive counterpart to surgical methods for stimulating the vagus.
For the active condition, stimulator electrodes deliver a mild electrical current to the tragus.
Stimulation parameters: stimulation of left tragus via two gold-plated electrodes, attached by ear-clip.
Waveform: rectangular, frequency: 20 Hz, pulse width: 0.2 ms, individually adjusted intensity based on participant's perceptual threshold.
Other Names:
Self-compassion imagery is both a meditative technique and a component of compassion-focused cognitive therapy.
Here, self-compassionate imagery is delivered as standardized audio-recorded instructions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
State self-compassion
Time Frame: 1 week
|
Self-compassion subscale of the scenario-based self-compassion and self-criticism Scales (SCCS; Falconer et al, 2015).
Score range: 15 (minimum) to 105 (maximum).
High scores indicate greater self-compassion (desirable outcome)
|
1 week
|
|
Heart rate variability
Time Frame: 1 week
|
Root mean square of successive differences (commonly, RMSSD) between normal beats; high-frequency power.
Higher levels indicate greater heart rate variability (a desirable outcome)
|
1 week
|
|
State self-criticism
Time Frame: 1 week
|
Self-criticism subscale of the SCCS (Falconer et al, 2015).
Score range: 15 (minimum) to 105 (maximum).
High scores indicate greater self-criticism (undesirable outcome)
|
1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Eye-tracking attention metrics
Time Frame: 1 week
|
Dwell time, first fixation and pupillometric indices of attentional bias to compassionate facial expressions (stimuli from Falconer et al., 2019).
Faces differ in intensity (25%, 50%, 75%, 100% compassion) versus matched neutral expression.
|
1 week
|
|
State mindfulness
Time Frame: 1 week
|
5 items (2 body, 2 mind, and 1 activity-related mindfulness items) from the State Mindfulness Scale (Tanay & Bernstein, 2013) as used by Shohan et al (2017).
The range (average across items) is 1 to 5, with high levels indicating greater state mindfulness (desirable outcome).
|
1 week
|
|
State positive and negative affect
Time Frame: 1 week
|
Positive affects subscale of the International positive and negative affect schedule-SF (iPANAS, 10 item version; Thompson, 2007).
Range of scores 5 (minimum) - 25 (maximum) for positive affect and 5-25 for negative affect, with higher scores indicating greater amounts of positive (desirable) and negative (undesirable) affect respectively.
|
1 week
|
|
State positive affect (Safe/content)
Time Frame: 1 week
|
Safe/content positive affect subscale of the Types of Positive Affect Scale (TPAS; Gilbert et al., 2008).
Range of scores: 0 (minimum) -16 (maximum), with higher levels indicating greater levels of 'safeness'/contentedness (desirable outcome)
|
1 week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sunjeev K Kamboj, PhD, UCL
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 07760/006
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Healthy Volunteers
-
AstraZenecaCompletedHealthy Elderly Volunteers | Healthy Young VolunteersUnited States
-
Syndax PharmaceuticalsCompletedHealthy Volunteers | Volunteers | Normal Volunteers | Human VolunteersUnited States
-
Syndax PharmaceuticalsCompletedHealthy Volunteers | Volunteers | Normal Volunteers | Human VolunteersUnited States
-
University Hospital, Clermont-FerrandUnite de Nutrition Humaine UMR 1019- INRAE; Unite MetaGenoPolis INRAE; France...CompletedHealthy Volunteers | Frail VolunteersFrance
-
Newcastle UniversityCompletedGI Glycaemic Index Healthy Volunteers | GL Glycaemic Load Healthy VolunteersUnited Kingdom
-
Galera Therapeutics, Inc.Syneos HealthCompleted
-
Galera Therapeutics, Inc.Syneos HealthCompletedHealthy | Healthy VolunteersAustralia
-
Galera Therapeutics, Inc.CelerionCompletedHealthy | Healthy VolunteersUnited States
-
Danone NutriciaCompletedHealthy Elderly | Healthy VolunteersChina
-
National and Kapodistrian University of AthensCompletedHealthy Adults | Healthy Volunteers OnlyGreece
Clinical Trials on Sham transcutaneous vagus nerve stimulation
-
Sahlgrenska University Hospital, SwedenRecruitingBorderline Personality DisorderSweden
-
Sheffield Teaching Hospitals NHS Foundation TrustRecruitingSubarachnoid Haemorrhage From Cerebral Aneurism RuptureUnited Kingdom
-
Northwell HealthCompletedStroke | Hemiparesis | Cerebrovascular Accident (CVA)United States
-
Max-Planck-Institute of PsychiatryRecruitingDepressive Disorder | Bipolar DisorderGermany
-
Wayne State UniversityNot yet recruitingPTSD - Post Traumatic Stress DisorderUnited States
-
Jiani WuRecruiting
-
Beijing Tiantan HospitalRecruitingHeadache | Unruptured Intracranial Aneurysm | Vagus Nerve StimulationsChina
-
Affiliated Hospital of Jiaxing UniversityNot yet recruiting
-
Guozhe SunCompletedCoronary Artery Disease | HypertensionChina
-
Guang'anmen Hospital of China Academy of Chinese...China Association for Science and TechnologyRecruiting