Clinical Trials Directory

Trials / Completed

CompletedNCT03914898

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

Effect of Nurse-Led Intervention Programme on Compassion Fatigue, Burnout, Compassion

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Dokuz Eylul University · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERNurse led intervention groupThis program is based on cognitive restructuring tecniques.

Timeline

Start date
2017-02-01
Primary completion
2017-04-30
Completion
2017-09-30
First posted
2019-04-16
Last updated
2020-12-08

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT03914898. Inclusion in this directory is not an endorsement.