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H-Senses Project - Self Care Mediated by the Senses

H-SENSES PROJECT Self Care Mediated by the Senses: Assessing the Impact on Self-esteem, Stress and Well-being of Female Health Professionals

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02406755
Enrollment
123
Registered
2015-04-02
Start date
2014-07-31
Completion date
2015-08-31
Last updated
2015-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Brief summary

Randomized clinical trial about self-care mediated by the senses in female health professionals and their influence on stress, self-esteem, mood states, life satisfaction and levels of salivary cortisol.

Detailed description

The work environment of health professionals is commonly considered stressful, given that they need to deal with difficult situations that include pain, risk of death, the decisions that need to be fast and accurate, and conflicts generated in interpersonal relationships. There is an ongoing discussion that the investigators need to care for those who care, however, there are few interventions studied and validated to effectively reduce the stress of these professionals that resonate in states of well-being. There is little room for discussion of this topic during the workday, as well as to learn techniques and measures for effective stress management. This study aims to explore the relationship between well-being, self-esteem and stress of women health professionals, and compare three self-care interventions mediated by the senses.

Interventions

OTHERone-sensory self care (Todo Dia®)

daily use of odorless body moisturizer (Todo Dia® - Natura)

OTHERmultisensory self care (Todo Dia®)

daily use of moisturizing body with cotton fragrance (Todo Dia® - Natura) + audiovisual stimulus

OTHERbi-sensory self care (Todo Dia®)

daily use of moisturizing body with cotton fragrance (Todo Dia® - Natura)

Sponsors

Hospital Israelita Albert Einstein
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Professional healthcare; * working in healthcare or administrative area in hospital * Voluntary participation; * Signed in term of free and informed consent.

Exclusion criteria

* Evaluation with relevant dermatological findings diagnosed by a dermatologist; * Work at nighttime or in alternate periods (because of known chronobiological changes that would affect the study of cortisol, one of the outcomes considered in the study); * who are breastfeeding; * Be pregnant

Design outcomes

Primary

MeasureTime frameDescription
Change in perceived stress (Lipp Stress Inventory and Symptoms of Stress List)baseline, 30 days, 60 daysLipp Stress Inventory and Symptoms of Stress List

Secondary

MeasureTime frameDescription
Change in cortisol levelsbaseline, 30 days, 60 daysSaliva will be collected to measure cortisol levels: 7-9 am

Other

MeasureTime frameDescription
Changes in Satisfaction with life (Satisfaction With Life Scale)baseline, 30 days, 60 daysSatisfaction With Life Scale
Changes in Positive and Negative Affectivebaseline, 30 days, 60 daysPositive and negative affect scale
Change in perceived self-esteem (Rosenberg's self-esteem Scale)baseline, 30 days, 60 daysRosenberg's self-esteem Scale

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026