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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02164188
Other study ID # HIAE_Florescer
Secondary ID
Status Completed
Phase N/A
First received April 29, 2014
Last updated August 9, 2017
Start date April 3, 2014
Est. completion date July 31, 2017

Study information

Verified date August 2017
Source Hospital Israelita Albert Einstein
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This protocol proposes a well-being program based on meditation and Positive Psychology principles such as human development, the improvement of virtues, quality of life and well-being. The investigators hypothesize that this program may promote well-being and reduce stress related problems in the participants. Objectives: To evaluate the efficacy of a well-being program in a sample of managers who work in a company (Natura Inovação/Cosméticos ) and health care professionals who work in a hospital (Hospital Israelita Albert Einstein) as well as its implication in the work environment. Methods: Sixty managers from Natura Inovação/Cosméticos and 60 health professionals from Hospital Israelita Albert Einstein will be recruited. The participants will be randomized in two groups of 30 participants each one, half of them in the control group (GC) and the other half to the intervention group (GI).


Description:

Introduction: Stress related disorders may lead to mental disorders as well as cardiovascular problems. They may also result in absenteeism and less productivity in companies. This protocol proposes a well-being program based on meditation and Positive Psychology principles such as human development, the improvement of virtues, quality of life and well-being. The investigators hypothesize that this program may promote well-being and reduce stress related problems in the participants. Objectives: To evaluate the efficacy of a well-being and quality of life program in a sample of managers who work in a company (Natura Inovação/Cosméticos ) and health care professionals who work in a hospital (Hospital Israelita Albert Einstein) as well as its implication in the work environment. Methods:Sixty participants from Natura Inovação/Cosméticos and 60 health professionals from Hospital Israelita Albert Einstein will be recruited. The participants will be randomized in two groups of 30 participants each one, half of them in the control group (GC) and the other half to the intervention group (GI). This is a cross-over study. After the first evaluation GI will participate in the Flourishing Program for 8 weeks and the GC will be a wait-list group in this period of time. After that, there is a second evaluation of the participants and the GC will receive the intervention (Flourishing Program). GI will not receive any intervention during this new period of 8 weeks. A final evaluation will happen after that. The participants will fill in questionnaires (to evaluate depression, anxiety, stress, positive and negative affects, sleep quality, self-compassion, mindfulness, virtues, values, happiness, psychological well-being) and will be clinically examined; their blood sample will be collected (for the dosage of health related biomarkers) and also saliva for cortisol measures. They will perform structural and functional neuroimaging exams (emotional and cognitive paradigms) and their physiological measures such as skin conductance will be recorded.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date July 31, 2017
Est. primary completion date July 31, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- Female aging from 25 to 60

- Managers from Natura Company or healthcare professionals from Hospital Israelita Albert Einstein

Exclusion Criteria:

- Sever mental or physical diseases

- For fMRI we will exclude participants who don´t match the criteria to undergoing this exam.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Flourishing protocol
This intervention is based on relaxation, well-being promotion, meditation practices, positive psychology principles. The format is 1hour and half meetings during 8 weeks, and daily practices. MP3 audios are presented for daily practices.

Locations

Country Name City State
Brazil Hospital Israelita Albert Einstein Sao Paulo

Sponsors (1)

Lead Sponsor Collaborator
Hospital Israelita Albert Einstein

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Other Changes in brain function Functional magnetic resonance imaging exams: emotional (International Affective Pictures System) and cognitive paradigms (Stroop Word Color Task and N-back). Baseline; 3 months; 6 months
Other Changes in anxiety symptoms Beck Anxiety Inventory baseline, 3 months,6 months
Other Changes in depression symptoms Beck Depression Inventory baseline, 3 months, 6 months
Other Changes in mindfulness Mindful Awareness Attention Scale baseline, 3 months, 6 months
Other Changes in Positive and Negative Affect PANAS questionnaire baseline, 3 months, 6 months
Other Changes in Psychological capital Psychological Capital Questionnaire baseline, 3 months, 6 months
Primary Change in perceived stress Lipp Stress Inventory; Perceived Stress Scale (baseline, 3 months, 6 months)
Primary Changes in well-being WHOQOL-bref (World Health Organization Quality of Life Questionnaire with 26 questions); Well-being at work scale; Psychological well-being scale. baseline, 3 months, 6 months
Secondary Change in cortisol levels Saliva will be collected to measure cortisol levels: 7-9 am, 4-5 pm, 11-12 pm. Baseline; 3 months; after 6 months
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