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Psychophysiological Responses to Six Single-Session Self-Regulation Interventions in a Female Adult With ADHD and Stabilized Bipolar Disorder

NCT ID: NCT07437833
Registry status: Recruiting
Study type: Interventional
Phase: Not applicable
Sponsor: Poznan University of Physical Education
Conditions: ADHD - Attention Deficit Disorder With Hyperactivity, Bipolar Affective Disorder; Remission in

Overview

ClinicalTrials.gov lists this study as Recruiting.

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

Enrollment: 1 participants (Estimated).

What is being studied

Intervention: Aftercare
Intervention: Aromatherapy
Behavioral: Aromatherapy
Intervention: Behavioral Disciplines and Activities
Intervention: Breathing Exercises
Intervention: Complementary Therapies
Intervention: Continuity of Patient Care
Behavioral: Cyclic Sighing
Behavioral: Emotional Freedom Technique Tapping
Intervention: Exercise
Intervention: Exercise Movement Techniques
Intervention: Mind-Body Therapies
Behavioral: Moderate-Intensity Aerobic Exercise on Cycloergometer
Intervention: Motor Activity
Intervention: Movement
Intervention: Musculoskeletal and Neural Physiological Phenomena
Intervention: Musculoskeletal Physiological Phenomena
Behavioral: Music Therapy
Intervention: Music Therapy
Intervention: Patient Care
Intervention: Physical Therapy Modalities
Intervention: Phytotherapy
Intervention: Psychotherapy
Intervention: Rehabilitation
Behavioral: Resting State (Control Session)
Intervention: Sensory Art Therapies
Intervention: Therapeutics
Behavioral: Virtual Reality Nature Immersion

Who may be eligible

Ages: 18 Years to 35 Years
Sex: Female
Healthy volunteers accepted: No

ClinicalTrials.gov lists the following 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).

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: Poland

Sample of listed locations

Poznan University of Physical Education — Poznan, Poland — Recruiting

Study details

Start date: July 31, 2026
Primary completion date: October 30, 2026
Completion date: October 30, 2026
First posted: February 27, 2026

Source and update information

Source: ClinicalTrials.gov
NCT ID: NCT07437833
Registry last updated: August 3, 2026
QualifiedStudies registry data refreshed: September 28, 2026
QualifiedStudies record fetched: September 28, 2026

View NCT07437833 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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