NCT07272031

Brief Summary

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.

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
11mo left

Started Jan 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress27%
Jan 2026Apr 2027

First Submitted

Initial submission to the registry

November 18, 2025

Completed
21 days until next milestone

First Posted

Study publicly available on registry

December 9, 2025

Completed
27 days until next milestone

Study Start

First participant enrolled

January 5, 2026

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2027

Last Updated

December 9, 2025

Status Verified

November 1, 2025

Enrollment Period

1.2 years

First QC Date

November 18, 2025

Last Update Submit

November 26, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change from Baseline in Morning Resting Heart Rate Variability (rMSSD) at 4 Weeks

    Baseline, Periprocedural and Week 4

  • Change from Baseline in Perceived Stress Level (PSS-10 Score) at 4 Weeks

    Baseline and Week 4

Secondary Outcomes (7)

  • Sleep Quality: Assessed using the Pittsburgh Sleep Quality Index (PSQI) total score

    Baseline and Week 4

  • General Self-Efficacy: Assessed using the General Self-Efficacy Scale (GSE) score

    Baseline and Week 4

  • Emotional Well-being: Assessed using the World Health Organization Well-being Index (WHO-5) score

    Baseline and Week 4

  • Neck Functional Limitation: Assessed using the Neck Disability Index (NDI) score

    Baseline and Week 4

  • Hand and Shoulder Functionality: Assessed using the Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire score

    Baseline and Week 4

  • +2 more secondary outcomes

Other Outcomes (6)

  • Age of Participants

    Baseline

  • Smoking Status Categories

    Baseline

  • Body Mass Index (BMI)

    Baseline

  • +3 more other outcomes

Study Arms (4)

Head Massage

ACTIVE COMPARATOR

Duration and Frequency: 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.

Procedure: Head Massage Intervention

Cervical Area Massage

ACTIVE COMPARATOR

Duration and Frequency: 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.

Procedure: Cervical Area Massage Intervention

Hand Massage

ACTIVE COMPARATOR

Duration and Frequency: 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.

Procedure: Hand Massage Intervention

Quiet Rest Control

PLACEBO COMPARATOR

Duration and Frequency: 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.

Other: Quiet Rest Control

Interventions

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.

Head Massage

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.

Cervical Area Massage

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.

Hand Massage

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.

Quiet Rest Control

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Una Veseta, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lead Researcher

Study Record Dates

First Submitted

November 18, 2025

First Posted

December 9, 2025

Study Start

January 5, 2026

Primary Completion (Estimated)

April 1, 2027

Study Completion (Estimated)

April 1, 2027

Last Updated

December 9, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will share