Improving Health of Nurses With Burnout Through Positive Psychological Intervention

August 31, 2018 updated by: Yuanhui Luo, Central South University

An Evaluation of Positive Psychological Intervention on Improving Health of Nurses With Burnout

Burnout is usually regarded as a response to chronic professional stressors like high workload, unfavorable emotion and complex interpersonal relationships. A high prevalence of burnout was found in many countries, and large-scale studies also showed high levels of burnout in Chinese nurses. As a stress-related syndrome, burnout was found to have detrimental influences on both psychological and physical health of nurses. Psychological problems such as depression and insomnia are verified to be associated with burnout. Endocrine dysfunction such as abnormal cortisol secretion rhythm occurred in shift-work nurses. Thyroid dysfunction was increasing and a sample of nurses were diagnosed with thyroid nodules and thyroid hormonal disorder during annual physical examination. Therefore, it is important to take measures to alleviate nurses' burnout to improve health.

Positive psychological interventions are defined as treatment methods or intentional activities to enhance person's positive emotions, cognitions and behaviours. In these methods and activities, people are usually required to finish a systematic exercise. According to a recent meta-analysis, Positive psychological interventions showed effectiveness in enhancing participants' well-being and reducing depressive symptoms. Therefore, this study aims to explore whether positive psychological intervention could reduce burnout and improve health of nurses.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

87

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hunan
      • Changsha, Hunan, China, 417600
        • Central South University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • officially employed licensed nurses; burnout score higher than 1.49; had a telephone on which WeChat could be installed.

Exclusion Criteria:

  • pregnant; current endocrine disorder; taking hormone drugs such as contraceptives.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group
Nurses with burnout are recruited in the intervention group and participate in positive psychological intervention.

Participants in the intervention group are required to record three good things every night before sleeping for five days a week using WeChat. Such things could be ordinary, minor or important.

WeChat is a common communication tool used in China, just like Facebook, basic messages could be sent individually and posting pictures or texts is also available.

No Intervention: Control group
Nurses with burnout are recruited in the control group and none interventions are conducted to them.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline Burnout at six months
Time Frame: The measurement was taken at baseline and six months.
Burnout of nurses is measured by Maslach Burnout Inventory-General Survey.
The measurement was taken at baseline and six months.
Change from Baseline Morning Plasma Cortisol at six months
Time Frame: The measurement was taken at baseline and six months.
The level of cortisol is assayed by using chemiluminescence method.
The measurement was taken at baseline and six months.
Change from Baseline Thyroid Related Hormones at six months
Time Frame: The measurement was taken at baseline and six months.
Triiodothyronine (T3), thyroxine (T4) and thyroid stimulating hormone (TSH) are assayed by using chemiluminescence method.
The measurement was taken at baseline and six months.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline Resilience at six months
Time Frame: The measurement was taken at baseline and six months.
Resilience of nurses is measured by Connor-Davidson Resilience Scale.
The measurement was taken at baseline and six months.
Change from Baseline Coping at six months
Time Frame: The measurement was taken at baseline and six months.
The level of coping among nurses is measured by Trait Coping Style Questionnaire.
The measurement was taken at baseline and six months.
Change from Baseline Self-efficacy at six months
Time Frame: The measurement was taken at baseline and six months.
The level of self-efficacy among nurses is measured by General Self-Efficacy Scale.
The measurement was taken at baseline and six months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2016

Primary Completion (Actual)

December 1, 2016

Study Completion (Actual)

December 1, 2016

Study Registration Dates

First Submitted

August 30, 2018

First Submitted That Met QC Criteria

August 31, 2018

First Posted (Actual)

September 5, 2018

Study Record Updates

Last Update Posted (Actual)

September 5, 2018

Last Update Submitted That Met QC Criteria

August 31, 2018

Last Verified

August 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 2015053

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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