Effect of Nurse-Led Intervention Programme Professional Quality of Life &

Status Completed

Clinical Trial Summary

Nurses are at risk in terms of burnout and empathic fatigue. Therefore, efforts to protect the mental health of nurses are very important. It is stated that the studies conducted are mostly descriptive and not interventional. In addition, the evidence levels of interventional studies are low.

Clinical Trial Description

Aim:The aim of this study is to reduce nurses' psychological distress, burnout and secondary trauma stress. Design This single-blind randomized controlled trial design was used. Measurements were made before, after and 6 months after Participants and Settings The study was perform at a hospital in Turkey. Intervention program was applied in 4 week. 84 nurses meeting the criteria were invited to the program.48 nurses agreed to participate. Nurses were randomly assigned groups. Sample Size the sample was calculated with the open epi program. The sample size was calculated as 20 per group. Intervention The program was created to reduce nurses' psychological distress, and improve the professional quality of life. The intervention programme were four sessions. The Intervention group was divided into two groups. Intervention were applied in a comfortable room in the hospital. Interventions were based on cognitive behavioral approach. Outcome measures The outcomes were compassion fatigue, burnout and compassion satisfaction, psychological distress. These variables were evaluated by the Professional Quality of Life Scale (ProQOL-IV). The GHQ-12 is a scale surveying psychological distress observed within the last few weeks. Data collection Research data were collected before, immediately after, and six months after intervention. Validity and reliability Measuring tools showing good psychometric properties were used to ensure validity and reliability. Volunteer participants were randomly assigned to groups, and the intention-to-treat approach was used for data analysis. The study has been reported in accordance with the CONSORT 2010 Statement principles. Ethical considerations Permission was obtained from the relevant university, and written permission was obtained from the hospital. The participants were informed, all participants gave written consent. Data analysis Mann Whitney U test, and Friedman analysis was used. All analyses were made on an intention-to-treat approach. Missing data were compensated for using the last observation method carried forward. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03914898
Study type	Interventional
Source	Dokuz Eylul University
Contact
Status	Completed
Phase	N/A
Start date	February 1, 2017
Completion date	September 30, 2017

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Effect of Nurse-Led Intervention Programme Professional Quality of Life and Psychological Distress in Nurses

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms