Office Massage Effects on HRV and Stress
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Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Head Massage Intervention, Cervical Area Massage Intervention, Hand Massage Intervention, Quiet Rest Control.
- Кому может быть актуально
- Состояния в реестре: Occupational Health, Autonomic Nervous System (ANS) Functioning and Mood State, Stress. Базовые параметры: от 18 лет · Женщины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Список центров уточняется — проверьте первичный протокол.
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Randomized Controlled Trial to Evaluate the Effectiveness of Three Different 15-Minute Office Massage Types (Head, Cervical Area, Hand) on Autonomic Nervous System Balance and Chronic Stress Reduction Using Heart Rate Variability (HRV)
Обзор
This study is a randomized controlled trial designed to investigate which of three short office massage types (head, neck/shoulder area, or hand) is most effective for reducing chronic stress in women who perform sedentary office work. Many sedentary female office employees experience long-term tension and work-related strain, which can affect the body's ability to recover. The investigators are testing whether a 15-minute massage, performed twice a week for four weeks, can help restore balance within the body. The investigators will evaluate the impact of these massages using Heart Rate Variability (HRV)-an objective measure that shows how well the body manages stress (autonomic nervous system balance)-as well as analyzing participants' self-reported levels of perceived stress, sleep quality, and overall well-being. Participants receiving massage will be compared to a control group engaging in quiet rest.
Вмешательства
- Процедура Head Massage Intervention
15 minutes per session, 2 times per week for 4 consecutive weeks (8 sessions total). Focus: Massage focuses on the scalp, temples, and auricles (outer ear) with the aim of stimulating cranial nerves, particularly branches of the vagus nerve. The procedure is performed by a licensed massage therapist while the participant is seated in an office chair. - Процедура Cervical Area Massage Intervention
15 minutes per session, 2 times per week for 4 consecutive weeks (8 sessions total). Focus: Deep tissue and kneading massage techniques applied primarily to the trapezius muscles, levator scapulae, and sub-occipital region (neck/shoulders). The procedure is performed by a licensed massage therapist while the participant is seated in an office chair. - Процедура Hand Massage Intervention
15 minutes per session, 2 times per week for 4 consecutive weeks (8 sessions total). Focus: Compression, rubbing, and stroking techniques applied to the palmar and dorsal surfaces of the hands, fingers, and wrists. The procedure is performed by a licensed massage therapist while the participant is seated in an office chair. - Другое Quiet Rest Control
Participants are seated in the same office chair for a structured 15-minute period, 2 times per week for 4 consecutive weeks (8 sessions total). Focus: Participants are instructed to sit quietly, avoid work-related activity, and refrain from using electronic devices. This arm controls for the effect of researcher attention and time spent away from work.
Первичные конечные точки
- Change from Baseline in Morning Resting Heart Rate Variability (rMSSD) at 4 Weeks [Срок оценки: Baseline, Periprocedural and Week 4]
- Change from Baseline in Perceived Stress Level (PSS-10 Score) at 4 Weeks [Срок оценки: Baseline and Week 4]
Вторичные конечные точки (7)
- Sleep Quality: Assessed using the Pittsburgh Sleep Quality Index (PSQI) total score [Срок оценки: Baseline and Week 4]
- General Self-Efficacy: Assessed using the General Self-Efficacy Scale (GSE) score [Срок оценки: Baseline and Week 4]
- Emotional Well-being: Assessed using the World Health Organization Well-being Index (WHO-5) score [Срок оценки: Baseline and Week 4]
- Neck Functional Limitation: Assessed using the Neck Disability Index (NDI) score [Срок оценки: Baseline and Week 4]
- Hand and Shoulder Functionality: Assessed using the Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire score [Срок оценки: Baseline and Week 4]
- Acute Pain Intensity Change: Assessed using the Numerical Rating Scale (NRS) score (0-10) in the specific massage area [Срок оценки: Periprocedural]
- Acute Subjective Well-being Change: Assessed using the Visual Analog Scale (VAS) (0-100 mm) for relaxation, fatigue, and tension [Срок оценки: Periprocedural]
Критерии участия
Критерии включения
Biological females aged 18 years or older. Currently working in an office job with at least 75% of the working day spent sitting (sedentary work).
Must report a regular menstrual cycle (cycle length 21-35 days) for at least the past 6 months.
Able to attend all scheduled intervention sessions (8 sessions over 4 weeks). Able to provide informed consent to participate in the study.
Критерии исключения
Use of hormonal contraceptives or other hormone-containing therapies (e.g., Intrauterine Device (IUDs), patches, birth control pills).
Pregnancy, current breastfeeding, or planning pregnancy during the study period.
Menopause (natural or surgically induced). Diagnosis of a severe chronic disease (e.g., heart failure, insulin-dependent diabetes, diagnosed neurological disorder).
Active cancer or history of cancer within the last 5 years. Current diagnosis of a major psychiatric disorder (e.g., major depressive disorder, bipolar disorder).
Current use of psychotropic medications that could significantly affect Heart Rate Variability (HRV) (e.g., certain beta-blockers, anti-depressants).
History of recent surgery (within the last 3 months) in the neck or upper extremities.
Participation in another clinical trial simultaneously.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Нерандомизированное
- Модель
- Параллельные группы
- Маскирование
- Простое слепое
- Основная цель
- Лечение
Центры проведения
Список центров уточняется — проверьте первичный протокол.
Идентификаторы
NCT: NCT07272031 · OM_HRV_2025_RCMC