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CompletedNCT02541747Updated Jul 12, 2016

Assessments in Stress and Quality of Sleep/Life in Night-shift Nurses and Doctors

A Phase 4 interventional study of massage in Shift-Work Sleep Disorder, sponsored by Taichung Veterans General Hospital. Completed at 1 site in Taiwan. Open to participants aged 20 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-07-12.

Sponsored by Taichung Veterans General Hospital · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
77
Allocation
Randomized
Ages
20 Years to 65 Years
Sex
All
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Study summary

This study aims to evaluate the effects of aroma massage to sleep quality of the nurses and staff during night shift.

Read the detailed description

Night shift increases physical and psychological pressure, and even affects their sleep quality. This study aims to evaluate the effects of aroma massage to sleep quality of the nurses during night shift after life-style modification and/or aroma massage. The investigators adopt a Randomized Controlled Trial (RCT) in this study. The investigators expect aroma massage would improve the sleep quality during night shift.

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Conditions studied

  • Shift-Work Sleep Disorder
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In context

Sleep Wake Disorders

788 studies on the registry are indexed under Sleep Wake Disorders; 186 are open to participants now.

This study's enrollment of 77 is above the median of 62 across 548 interventional studies indexed under Sleep Wake Disorders.

Browse Sleep Wake Disorders studies →

Lead sponsor

Taichung Veterans General Hospital is the lead sponsor of 171 studies on the registry; 38 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Shift-Work Nurses and Staff

Exclusion criteria

Exclusion Criteria:

  • Diabetes mellitus, cardiovascular disease and psychological disorders
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
77 participants (actual)

Study arms

  • Active comparator
    massage

    massage for 30 min, once a week for 4 weeks

    Behavioral: massage

  • No intervention
    control

    Rest as control

Interventions

  • Behavioralmassage

    massage

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What researchers measure

Primary outcomes

  1. brain-derived neurotrophic factor

    Time frame: 4 weeks

Secondary outcomes

  1. Pittsburgh sleep quality index (PSQI)

    Psychological questionnaire

    Time frame: 4 weeks

  2. Depression score ( Zung's Self-Reported Depression Scale)

    Psychological questionnaire- Zung's Self-Reported Depression Scale

    Time frame: 4 weeks

  3. Anxiety score (Beck Anxiety Inventory)

    Psychological questionnaire- Beck Anxiety Inventory

    Time frame: 4 weeks

  4. Heart rate variability

    Cardiopulmonary functions

    Time frame: 4 weeks

  5. Metabolic syndrome (NCEP)

    Third Report of the National Cholesterol Education Program (NCEP) criteria

    Time frame: 4 weeks

  6. VCAM-1

    Cardiovascular risk and Inflammatory markers

    Time frame: 4 weeks

  7. Irisin

    Cardiovascular risk and Inflammatory markers

    Time frame: 4 weeks

  8. circadian rhythm

    orexin

    Time frame: 4 weeks

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Study locations

1 site
  • Division of Endocrinology and Metabolism, Department of Internal Medicine, Taichung Veterans General Hospital
    Taichang, 407, Taiwan
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 12, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02541747
Lead sponsor
Taichung Veterans General Hospital
Responsible party
Sponsor
First posted
Sep 4, 2015
Start date
Jun 2014
Primary completion
Jun 2015
Completion
Jun 2015
Last update
Jul 12, 2016

Study contacts

Wayne HH Sheu, MD, PhD
principal investigator · Taichung Veterans General Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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