Psychophysiological Responses to Six Single-Session Self-Regulation Interventions in a Female Adult With ADHD and Stabilized Bipolar Disorder
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Moderate-Intensity Aerobic Exercise on Cycloergometer, Cyclic Sighing, Aromatherapy, Music Therapy.
- Who it may be relevant to
- Registry conditions: ADHD - Attention Deficit Disorder With Hyperactivity, Bipolar Affective Disorder; Remission in. Basic parameters: 18 years — 35 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Poland
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Psychophysiological Responses to Six 15-Minute Single-Session Self-Regulation Interventions in a Female Adult With ADHD and Stabilized Bipolar Disorder: A Single-Case Study
Overview
This study aims to explore how six short, 15-minute self-regulation techniques affect the body and brain in a female adult with ADHD and stabilized bipolar disorder. The techniques being tested include: * Aerobic exercise * Controlled breathing (cyclic sighing) * Aromatherapy with lavender essential oil * Listening to specific music (Solfeggio 528 Hz) * Virtual reality relaxation with forest imagery * Emotional Freedom Technique (EFT) tapping One session of quiet sitting with eyes open serves as a comparison. The participant will attend one 15-minute session per week for each technique. Before and after each session, the researchers will measure: * Heart rate and heart rate variability * Stress levels using Subjective Units of Distress Scale * Mood using a questionnaire * Blood pressure * Brain activity using EEG * Memory performance with a simple test (N-back) * Pain sensitivity The goal is to understand how these short, non-invasive techniques influence both physiological and psychological responses. Sessions are safe, short, and designed to involve minimal risk. The findings may help guide future research on relaxation and exercise strategies for people with ADHD and bipolar disorder.
Interventions
- Behavioral Moderate-Intensity Aerobic Exercise on Cycloergometer
The participant performs a 15-minute session of moderate-intensity cycling on a stationary ergometer. Moderate intensity is defined as 64-76% of maximum heart rate according to ACSM guidelines. The exercise load is set to 2 watts per kilogram of body weight. Heart rate is monitored using a Polar chest strap. - Behavioral Cyclic Sighing
The participant performs cyclic sighing for 15 minutes while sitting in a chair. They inhale slowly, and once the lungs are expanded, perform a second inhale to maximally fill the lungs, even if the second inhale is shorter or smaller in volume than the first. They then slowly and fully exhale all their breath. The participant performs all inhales and exhales through the nose. - Behavioral Aromatherapy
The participant undergoes a 15-minute aromatherapy session while sitting comfortably in a chair in a closed room (2 m × 4 m). Lavender essential oil is diffused into the air using an aroma diffuser placed approximately 1 meter from the participant. The participant breathes normally and does not perform controlled breathing. - Behavioral Music Therapy
The participant listens to 528 Hz solfeggio frequency music for 15 minutes while seated comfortably in a quiet, closed room. Music is delivered through headphones or a speaker at a comfortable volume. - Behavioral Virtual Reality Nature Immersion
The participant wears a VR headset and views a 15-minute immersive forest and nature environment while seated comfortably in a quiet, closed room. The VR experience includes visual and auditory elements of a natural forest scene. - Behavioral Emotional Freedom Technique Tapping
The participant performs a 15-minute Emotional Freedom Technique (EFT) tapping session while seated comfortably in a quiet, closed room. The participant taps on standardized acupressure points in the following order: karate chop (side of hand), inner eyebrow, side of eye, under eye, under nose, chin, collarbone, under arm, and top of head. Each point is tapped 10-15 times with steady, moderate pressure. - Behavioral Resting State (Control Session)
The participant sits quietly in a chair with eyes open for 15 minutes in a calm, closed room. No active intervention, tapping, breathing exercises, music, aromatherapy, or virtual reality is administered during this session. The participant is instructed to remain seated with eyes open maintaining a natural posture without engaging in any structured activity.
Primary outcome measures
- Mean EEG spectral power in theta, alpha, low beta, high beta, gamma frequency bands during resting-state (eyes-open and eyes-closed) [Time frame: Baseline: immediately before intervention; Post-intervention: immediately after completion of the intervention period]
- Heart Rate Variability (HRV) [Time frame: Baseline (average over 5-minute resting-state immediately before intervention); During intervention (average over entire session, periprocedural); Post-intervention (average over 5-minute resting-state immediately after intervention).]
Secondary outcome measures (8)
- Mean EEG spectral power in theta, alpha, low beta, high beta, and gamma frequency bands during N-back task [Time frame: Baseline (during N-back task immediately before each intervention session, periprocedural); Post-intervention (during N-back task immediately after each intervention session, periprocedural)]
- Mean EEG spectral power in theta, alpha, low beta, high beta, and gamma frequency bands during intervention session [Time frame: During intervention session (periprocedural, averaged over entire session).]
- Perceived Stress measured with the Subjective Units of Distress Scale (SUDS) [Time frame: Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention session]
- Cognitive Performance (N-back) [Time frame: Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention session.]
- Blood Pressure [Time frame: Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention session]
- Pain Threshold [Time frame: Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention session.]
- Positive and Negative Affect measured with the Positive and Negative Affect Schedule - Short Form (PANAS-SF) [Time frame: Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention session]
- Heart Rate [Time frame: Baseline: immediately before each intervention session; Post-intervention: immediately after each intervention session.]
Eligibility criteria
Inclusion criteria
- Diagnosis of ADHD and bipolar disorder (type I or II) in stable remission.
- No active depressive, manic, or psychotic episodes for at least 2 years.
- No use of psychotropic medications, including mood stabilizers, antidepressants, antipsychotics, or ADHD medications, for at least 2 years.
- No chronic somatic diseases (including neurological, cardiovascular, or metabolic disorders).
- Regular sleep-wake rhythm during the week preceding the study.
- Non-smoker.
- No night-shift work in the week preceding the study.
Exclusion criteria
- Acute medical conditions that could affect study procedures.
- Use of medications in the past 3 months that influence cardiovascular or neurological parameters.
- Consumption of alcohol or psychoactive substances on the day before or day of the study.
- Intense physical activity on the day before or day of the study.
- Contraindications to moderate-intensity exercise on a cycle ergometer (e.g., recent injuries, chronic musculoskeletal conditions).
- Contraindications to EEG measurement (e.g., scalp skin conditions preventing proper electrode placement, hypersensitivity to conductive gels or pastes).
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
Poland · 1 center
- Poznan University of Physical Education — Poznan
Identifiers
NCT: NCT07437833 · 716/25_2