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Acute Effects of a Single-Session Body Awareness Intervention on Cortical Activity and Interoceptive Accuracy

Investigation of the Acute Effects of a Body Awareness Application on Cortical Activity and Interoceptive Accuracy in Healthy Young Adults

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07736365
Acronym
BBAT-EEG
Enrollment
84
Registered
2026-07-30
Start date
2026-09-01
Completion date
2028-03-31
Last updated
2026-07-30

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

Conditions

Healthy Volunteers - Male and Female

Keywords

body awareness, basic body awareness therapy, interoception, EEG, cortical activity, heartbeat perception

Brief summary

This study will examine the immediate (acute) effects of a single, 30-minute body awareness session on brain activity and interoceptive accuracy in healthy young adults aged 18-25. Participants will be randomly assigned to one of two groups: an intervention group, which will complete a structured body awareness exercise based on Basic Body Awareness Therapy, or a control group, which will rest quietly for the same amount of time without any specific instructions. Before and after the session, brain activity will be recorded using a portable, 8-channel EEG device, and interoceptive accuracy will be measured with a heartbeat perception task, in which participants try to count their own heartbeats without checking their pulse. The main goal is to determine whether a single body awareness session produces measurable changes in EEG brain wave patterns (theta, alpha, beta, and gamma bands) and in the accuracy of heartbeat perception, and whether these two types of change are related to each other.

Detailed description

Body awareness is a multidimensional construct that involves conscious perception of posture, breathing, muscle tone, movement, balance, contact, and internal bodily sensations. It is closely related to interoception - the perception and interpretation of physiological signals arising from within the body. Prior research suggests that body-awareness-based approaches, such as Basic Body Awareness Therapy, can positively influence body awareness, body attitude, and psychophysiological function in various clinical populations. However, few studies have examined the acute neurophysiological effects of a single body awareness session in healthy young adults using portable, low-channel EEG systems, and the relationship between EEG changes and interoceptive accuracy remains insufficiently explored. This study is designed as a two-arm, parallel-group, randomized controlled trial. Participants will be randomly assigned in a 1:1 ratio to either an intervention group or a control group. Randomization will be generated by an independent researcher not involved in data collection or intervention delivery, using a computer-based random number method; group allocation will be concealed using sequentially numbered, opaque, sealed envelopes opened only after baseline measurements are completed. Due to the nature of the intervention, participants and the person delivering the session cannot be blinded; however, researchers involved in EEG signal processing and interoceptive accuracy scoring will be blinded to group assignment where possible. The intervention group will receive a single, approximately 30-minute structured body awareness session based on Basic Body Awareness Therapy principles, consisting of preparatory orientation, supine body scanning and contact awareness, breath awareness, slow symmetrical movement awareness, seated midline/postural awareness, standing weight-shift awareness, and a closing integration period. The control group will undergo a quiet/neutral resting session of equal duration and in the same environment, without any body-awareness-related instructions, in order to control for effects attributable to time, environment, rest, or eye closure alone. In both groups, resting-state EEG will be recorded before and after the session using an 8-channel wireless EEG device (Enobio 8) at a 500 Hz sampling rate, following the international 10-20 system, with electrode sites covering frontal, sensorimotor, and parietal regions (Fz, FCz, Cz, C3, C4, Pz, P3, P4). EEG data will be preprocessed using standard steps including band-pass filtering (1-45 Hz), 50 Hz notch filtering, independent component analysis (ICA), artifact rejection, and common average referencing. Absolute and relative power in the delta, theta, alpha, beta, and gamma frequency bands will be calculated, with particular attention to frontal theta, alpha, and gamma activity, given their proposed associations with attention, internal focus, and relaxation. Interoceptive accuracy will be assessed before and after the session using a heartbeat perception task based on the Schandry method, in which participants silently count perceived heartbeats over defined time intervals without taking their pulse; actual heartbeats will be recorded physiologically over the same intervals, and a normalized interoceptive accuracy score will be derived from the agreement between perceived and actual counts. The primary outcome is the pre-to-post change in EEG frequency band power. The secondary outcome is the pre-to-post change in interoceptive accuracy score, and the relationship between EEG-based changes and interoceptive accuracy changes will also be examined. Sample size was determined via power analysis (G\*Power 3), based on effect sizes reported in prior heartbeat-evoked potential research, yielding a target of 42 participants per group (84 total) at α = 0.05 and 80% power, including an allowance for a 20% dropout rate. Statistical analysis will include mixed-design analyses (e.g., two-way mixed ANOVA or linear mixed models) to evaluate group × time interactions for EEG outcomes, and correlational analyses (Pearson or Spearman) to examine associations between EEG and interoceptive accuracy changes, with appropriate corrections for multiple comparisons across channels and frequency bands. The study will be conducted and reported in accordance with CONSORT guidelines for randomized controlled trials.

Interventions

OTHERBasic Body Awareness Therapy Intervention

A single \~30-minute body awareness session delivered in a quiet, well-ventilated room with minimal distraction. The session follows a structured sequence of low-intensity, pain-free, non-strenuous body awareness exercises performed in supine, sitting, and standing positions, guided verbally by a trained physiotherapist or researcher. The session focuses on conscious awareness of posture, contact points, breathing, and movement quality rather than physical performance, strength, or flexibility. Participants are instructed to move without forcing and to report any pain, dizziness, or discomfort during the session.

OTHERNo Intervention/Sham Comparator

A single \~30-minute quiet resting session delivered in the same room and under the same environmental conditions as the intervention session. Participants will be asked to remain in a comfortable seated or supine position, close their eyes or fix their gaze on a stationary point, and rest quietly for the full duration. No specific breathing, body awareness, or movement instructions will be given. Participants will be informed that they may notify the researcher if they experience any discomfort.

Sponsors

Ertugrul Deniz Kose
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

Participants and the person delivering the intervention/control session cannot be blinded to group assignment due to the nature of the intervention. However, outcome assessors - specifically, the researchers responsible for EEG signal preprocessing, feature extraction, and interoceptive accuracy scoring - will be blinded to group allocation. Group codes will be masked during data analysis to minimize assessment and analytic bias.

Intervention model description

Participants will be randomly assigned in a 1:1 ratio to one of two parallel groups: an intervention group receiving a single structured body awareness session, or a control group receiving a quiet/neutral resting session of equal duration. Both groups will undergo identical pre- and post-session EEG recordings and interoceptive accuracy assessments, allowing within-group (pre-post) and between-group comparisons of change.

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-25 years * Self-reported healthy status * Literate in Turkish * Willing and able to provide written informed consent

Exclusion criteria

* Active epilepsy or seizure history * Diagnosed psychiatric disorder * Neurological disorder * Cardiac arrhythmia, pacemaker, heart disease * Active use of psychotropic, beta-blocker, anticholinergic, or antihistamine medication * Prior participation in Basic Body Awareness Therapy * Pregnancy * Active scalp lesion or dermatological pathology * Neurological/psychiatric medication affecting alertness or attention * Alcohol consumption in the last 24 hours * Excessive caffeine intake on the day of measurement * Acute pain, fever, infection, or other condition that could affect measurement

Design outcomes

Primary

MeasureTime frameDescription
Change in EEG Theta Band PowerImmediately before vs. immediately after the ~30-minute sessionAbsolute power (µV²) in the theta frequency band (4-8 Hz), calculated from EEG recordings before and after the body awareness intervention.
Change in EEG Alpha Band PowerImmediately before vs. immediately after the ~30-minute sessionAbsolute power (µV²) in the alpha frequency band (8-13 Hz), calculated from EEG recordings before and after the body awareness intervention.
Change in EEG Beta Band PowerImmediately before vs. immediately after the ~30-minute sessionAbsolute power (µV²) in the beta frequency band (13-30 Hz), calculated from EEG recordings before and after the body awareness intervention.
Change in EEG Gamma Band PowerImmediately before vs. immediately after the ~30-minute sessionAbsolute power (µV²) in the gamma frequency band (30-45 Hz), calculated from EEG recordings before and after the body awareness intervention.

Secondary

MeasureTime frameDescription
Change in interoceptive accuracy scoreImmediately before vs. immediately after the ~30-minute sessionInteroceptive accuracy will be measured using a normalized accuracy score derived from the Schandry heartbeat perception task, ranging from 0 to 1, where higher scores indicate greater accuracy in perceiving one's own heartbeat (i.e., better interoceptive accuracy).

Contacts

CONTACTErtuğrul Deniz Köse, Ph.D
ertugrul.kose@amasya.edu.tr+905056740998
CONTACTEylem KÜÇÜK, Ph.D
eylem.kucuk@amasya.edu.tr+905067025859
PRINCIPAL_INVESTIGATORErtuğrul Deniz Köse, Ph.D

Amasya University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026