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OpenTrials
Completed

NCT Number: NCT02387528

Efficacy of a Mindfulness-Based Intervention Versus Relaxation in Primary Care Burnout Providers.

The prevalence of the Burnout Syndrome (BS) or symptoms among Primary Health Care (PHC) providers is high and can affect their quality of life and clinical results. Mindfulness-based interventions (MBI) have been tested as promising interventions to manage chronic stress and BS in PHC providers.

The main goal of this study was to compare the efficacy of an eight week MBI (Group 1 or G1) on burnout symptoms in Brazilian PHC providers, compared to a briefer, four-week relaxation-based intervention (Group 2 or G2) and to a waiting list control group (Group 3 or G3). The initial hypothesis was that the MBI is superior to relaxation and to the waiting list group. A non-randomized controlled trial was performed, with mixed-methods evaluation (qualitative and quantitative).

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Marcelo Marcos Piva Demarzo

São Paulo, Brazil

About this study

Study Design: a non-randomized pragmatic controlled trial was performed, with mixed-methods investigation.

Population: The target population of the study were PHC professionals from the city of Porto Alegre in the southern region of Brazil.

Sample: PHC professionals from 50 health units. A sample size calculation was performed, considering an effect size of 0.5 (moderate), with a statistical power of 80% and a confidence interval of 95%. Thus, 65 individuals in each group would be necessary, totaling 195 people distributed in the three groups, estimating a drop-out rate of 10%.

Inclusion criteria

18 years or over, complete primary education at least, be interested in the objectives of this study and have consented to volunteer to participate in one of the three groups of interventions proposed, being a primary health care worker for at least six months and experiencing any kind of stress in relation to work.

Exclusion criteria

Have been practicing mindfulness, meditation, yoga or similar (tai chi chuan, qi gong) in the last six months, presence of diagnosed clinical diseases that would not allow adherence to the study, being in treatment for psychological or psychiatric problems, in the phase of therapeutic adjustment (less than three months of psychological or pharmacological interventions), be on medical leave of absence from work, dependence or abusive use of alcohol or other drugs, except for tobacco.

Recruitment and procedures: The study was publicized among all PHC units using informative pamphlets, and PHC managers were informed personally by the first author (DS) about the goals of the project. The professionals were dismissed during working hours for the meetings that took place in places available and previously scheduled with the heads of health services. All the volunteers were previously submitted to the study´s criteria for participation. Those who were interested underwent a brief evaluation using the Beck´s Depression Inventory (BDI), Self Reported Questionnaire (SRQ-20) (common mental disorders) and Self Reported Questionnaire (SRQ-A) (alcohol use) scales to exclude severe symptoms (suicidal ideation and alcohol abuse). After inclusion, volunteers were able to choose between the three participant groups of the study (mindfulness, relaxation, or waiting list). We did not randomize the professionals in order to make the study more feasible and pragmatic. Specifically, in a pilot study we had observed that the professionals were highly resistant to being randomly allocated to the study groups.

Ethics: This study was conducted according to the Declaration of Helsinki and was submitted to three Research Ethics Committees, respecting all the criteria for the execution of research with human beings.

All participants agreed to participate in the study and signed the Free and Informed Consent prior to any study procedure.

A drop-out was defined as a participant who completed fewer than four sessions.

Measures:

Added to sociodemographic data, the Maslach Burnout Inventory - General Survey) (MBI-GS ) was used to identify symptoms of BS, The Positive and Negative Scale (PANAS) to evaluate affection, Five Facet Mindfulness Questionnaire (FFMQ) to measure mindfulness dimensions; the Experience Scale to measure decentering and rumination (ES), and the Self-Compassion Scale (SCS) to measure compassion.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Volunteers over 18 years old who consent to be randomized to one of two groups, and
  • have available time to join the research

Exclusion criteria

  • Practitioners of mindfulness, meditation yoga or similar in last year,
  • presence of not controlled greater severity diseases, such as cancer, schizophrenia, epilepsy, or other psychiatric diseases,
  • alcohol or other drugs addiction or abuse, except tobacco, and
  • being in acute treatment for psychological or psychiatric problems. All volunteers will undergo a brief initial clinical evaluation to assess whether the conditions of mental and physical health permit participation in groups.

Treatment and study plan

1- Mindfulness Intervention

Behavioral

An intervention program integrating elements of Mindfulness Breathworks Institute Mindfulness based approaches for Pain and illness (MBPI), (Burch , 2009) and Mindfulness Based Stress Reduction (MBSR), (Kabat Zinn, 2003), and Mindfulness based Cognitive Therapy (MBCT) shall be used. All programs are highly structured, lasting eight weeks, with a weekly meeting about two hours , and working with four main techniques during these meetings : mindfulness in breathing, body scan, walking meditation and mindfulness yoga. In order to facilitate the home practice of meditation by participants during and after the intervention protocol, all will receive a CD containing guided meditation sessions, covering the above techniques.

Other names: Mindfulness Based Stress Reduction

2- Relaxation Intervention

Behavioral

Eight meetings where the participants will practice relaxation techniques.

Other names: Relaxation

3- Wait List Control Group

Other

No intervention

Other names: Wait List

Primary outcomes

  1. A mindfulness intervention decreases burnout symptoms

    Time frame: up to 2 months

    Measured by MBI-GS.

Secondary outcomes

  1. A mindfulness intervention decreases negative affect and increases positive affect

    Time frame: up to 2 months

    After the intervention, measured by PANAS

  2. A mindfulness intervention improves self compassion

    Time frame: up to 2 months

    measured by SCE after intervention.

  3. A mindfulness intervention Increases mindfulness state.

    Time frame: up to 2 months

    measured by FFMQ

  4. A mindfulness intervention improves decentering and decrease cognitive rumination

    Time frame: up to 2 months

    Measured by ES - Experience scale

Sponsors and collaborators

Lead sponsor

Federal University of São Paulo

Other

Collaborators

  • Federal University of Rio Grande do Sul

Registry information

Official study title

Efficacy of a Mindfulness-Based Intervention ("Breathworks for Stress") Versus Relaxation in the Symptoms of Burnout in Primary Care Providers: A Mixed-Methods Pragmatic Controlled Study

Acronym: MINDFULNESS

Important dates

Study start
2014
Primary completion
2014
Study completion
2018
First posted
Mar 13, 2015
Registry last updated
Mar 29, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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