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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.
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Inclusion criteria
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.
Exclusion criteria
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.
Primary purpose
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Interventional model
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140 participants in 4 patient groups, including a placebo group
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Central trial contact
Una Veseta, PhD
Data sourced from clinicaltrials.gov
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