Skip to content

Evaluation of the Effect of Cognitive Behavioral Approach-Based Stress Coping Skills Training Program on Stress Perception, Resilience and Compassion Fatigue

Evaluation of the Effect of Cognitive Behavioral Approach-Based Stress Coping Skills Training Program Performed by Tele-Nursing on Stress Perception, Resilience and Compassion Fatigue in Palliative Care Nurses

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05830448
Enrollment
42
Registered
2023-04-26
Start date
2021-11-12
Completion date
2023-10-12
Last updated
2023-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress Perception, Psychological Resilience, Compassion Fatigue

Keywords

palliative care nurses, Stress, Stress Perception, Ability to Cope with Stress, Psychological Resilience, Compassion Fatigue

Brief summary

This research is an experimental study with a randomized pre-test-post-test control group to evaluate the effect of the cognitive behavioral approach-based stress coping skills training program carried out by tele-nursing on the palliative care nurses' perception of stress, resilience and compassion fatigue. The main questions it aims to answer are: Question 1. Will the cognitive behavioral approach-based stress coping skills training program to be carried out through tele-nursing have an effect on the increase in the stress coping score of the palliative care nurses in the intervention group? Question 2. Will the cognitive behavioral approach-based stress coping skills training program to be carried out through tele-nursing have an effect on the reduction of stress perception among palliative care nurses in the intervention group? Question 3. Will the cognitive behavioral approach-based stress coping skills training program to be carried out through tele-nursing have an impact on the increase in resilience of palliative care nurses in the intervention group? Question 4. Will the cognitive behavioral approach-based stress coping skills training program to be carried out through tele-nursing have an effect on the reduction of compassion fatigue in palliative care nurses in the intervention group? The research was planned as a randomized controlled experimental design with the required ethics committee and institution permissions, a three-month announcement and initiation period, and an eight-week intervention period. Data will be collected twice at baseline and after intervention (Week 9). Personal information form, Perceived Stress Scale, Coping with Stress Scale, Connor-Davidson Resilience Scale, Quality of Life Scale for Employees will be used in the pre-test phase of data collection. Participants meeting the inclusion criteria will be assigned to the intervention and control groups by randomization. In order to support nurses in the intervention group to gain awareness of stress and anxiety and develop positive coping skills with stress, a total of 8 sessions of 40 minutes are planned, including interaction steps based on education and cognitive approach. Individuals will be given homework from the second week and they will be asked to deliver these homeworks to the researcher 2 days before the next interview, and it is planned to send reminder messages from the WastApp group created. Participants who do not deliver the assignments given in this study to the researcher on time will be excluded from the research even if they participate in online training. No intervention will be applied to individuals assigned to the control group. Participants will be informed about the Mobile Mental Health Support System created by the Turkish Ministry of Health and will be directed to this application. It is planned to apply Perceived Stress Scale, Coping with Stress Scale, Connor-Davidson Resilience Scale, Quality of Life Scale for Employees at the 9th week for the application of post-tests.

Interventions

BEHAVIORALCognitive Behavioral Therapy

The trial was planned to have a three-month announcement and an eight-week intervention period. Personal information form, Perceived Stress Scale, Coping with Stress Scale, Connor-Davidson Resilience Scale, Quality of Life Scale for Employees will be used in the pre-test phase of data collection. Participants meeting the inclusion criteria will be randomly assigned to the intervention and control groups. In order to support nurses in the intervention group to gain awareness of stress and anxiety and develop positive coping skills, 8 sessions of 40 minutes were planned, including interaction steps based on education and cognitive approach. As of the second week, homework will be given to individuals and they will be asked to submit these assignments to the researcher 2 days before the next interview. Participants who do not submit the assignments given in this study to the researcher on time will be excluded from the study even if they have completed the training.

BEHAVIORALT.R. Mobile Mental Health Support System produced by the Ministry of Health

No intervention will be applied to the individuals assigned to the control group by the researcher. Participants will be informed about the Mobile Mental Health Support System created by the Turkish Ministry of Health and will be directed to this application.

Sponsors

Eskisehir Osmangazi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

The nurses to be included in the study will be assigned to the intervention and control groups by simple randomization using the computer-assisted randomization application (www.randomizer.org). Determination of the intervention and control group will be drawn between set1 and set2. The ranking to be given to the participants (eg 1,2,3,….32) will be created by recording the number of participants when they approve to participate in the research (eg, the 10th person who accepts to participate will automatically be the 10th participant). No new applications will be accepted when the number of people to be included in the sample is reached. Participants in the study will not know which group they belong to. The researcher will contact the individual assigned to the control and intervention group according to the number given without knowing who the participant is. Blinding will be provided by Outcomes Assessor during data entry and statistics stages.

Intervention model description

Experimental study with randomized pretest-posttest control group

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Working as a nurse in designated hospitals in Eskişehir, * To have been working in palliative care services for at least one month, * Having active internet access and being able to actively use a computer/tablet or smart phone. * Volunteering to participate in the research.

Exclusion criteria

* Working in hospitals located in other provinces of Turkey, * Working in all units in hospitals except the palliative care service, * Having any psychiatric diagnosis other than stress, * Being currently receiving psychological counseling,

Design outcomes

Primary

MeasureTime frameDescription
Perceived Stress Scale5 monthsThe stress perception of the nurses working in the palliative care service will be evaluated. The minimum score that can be obtained from the perceived stress scale is 0, and the maximum score is 56. A higher score on this scale means a worse result.
Connor-Davidson Resilience Scale5 monthsThe psychological resilience levels of the nurses working in the palliative care service will be evaluated. The minimum score that can be obtained from the Connor-Davidson Resilience scale is 0, and the maximum score is 100. A higher score on this scale means a better result.
Quality of Life Scale for Employees - Compassion Fatigue Sub-Dimension5 monthsInformation about compassion fatigue of nurses working in palliative care service will be given. The minimum score that can be obtained from the Employee Quality of Life Scale - Compassion Fatigue Sub-Dimension is 0, and the maximum score is 50. A higher score on this scale means a worse result.

Countries

Turkey (Türkiye)

Contacts

Primary ContactOZGE AYDOGAN ASIR
aydogan.ozge.92.123@gmail.com05076239241
Backup ContactOZLEM ORSAL

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026