- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03657563
Improving Health of Nurses With Burnout Through Positive Psychological Intervention
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
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hunan
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Changsha, Hunan, China, 417600
- Central South University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
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
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.
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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.
|
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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.
|
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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.
|
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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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015053
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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