Narrative Group Counseling and Psychological Resilience
The Effect of Narrative Group Counseling on Psychological Resilience in Nursing Students
1 other identifier
interventional
68
1 country
1
Brief Summary
This study aims to examine the effect of narrative group counseling applied to nursing students studying at a public university on psychological resilience. The research was used parallel group, randomized, controlled experimental design. According to the power analysis results, the sample size was determined to be at least 54 people. Due to possible losses, 25% more people were included in the study and 68 students who met the inclusion criteria were assigned to the intervention (n = 34) and control group (n = 34). In the study, the assignment of students to the intervention and control groups were made by stratified randomization(gender,class). Due to the fact that nursing department courses continued all day on weekdays, limited transportation and winter conditions, students from the intervention group (n = 7) and the control group (n = 5) did not want to continue the sessions. The implementation of the research was completed with a total of 56 students, with n=27 in the intervention group and n=29 in the control group. Personal information forms and Adult Resilience Scale were used to obtain research data. The data collection process was carried out in four stages: pre-test, post-test, 3-month follow-up test and 6-month follow-up test.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 13, 2023
CompletedFirst Submitted
Initial submission to the registry
November 14, 2023
CompletedFirst Posted
Study publicly available on registry
November 18, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 8, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2024
CompletedJuly 15, 2024
July 1, 2024
2 months
November 14, 2023
July 12, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Resilience Scale For Adults (RSA)
Resilience Scale for Adults The Turkish validity and reliability of the scale developed by Fribourg et al. (2003) was conducted by Basım and Çetin (2011). The 33-item scale consists of six sub-dimensions: "Self-Perception", "Future Perception", "Structural Form", "Social Competence", "Family Cohesion" and "Social Resources".
before the intervention
Resilience Scale For Adults (RSA)
Resilience Scale for Adults The Turkish validity and reliability of the scale developed by Fribourg et al. (2003) was conducted by Basım and Çetin (2011). The 33-item scale consists of six sub-dimensions: "Self-Perception", "Future Perception", "Structural Form", "Social Competence", "Family Cohesion" and "Social Resources".
eight weeks after the start of intervention
Resilience Scale For Adults (RSA)
Resilience Scale for Adults The Turkish validity and reliability of the scale developed by Fribourg et al. (2003) was conducted by Basım and Çetin (2011). The 33-item scale consists of six sub-dimensions: "Self-Perception", "Future Perception", "Structural Form", "Social Competence", "Family Cohesion" and "Social Resources".
three months after implementation of the intervention
Resilience Scale For Adults (RSA)
Resilience Scale for Adults The Turkish validity and reliability of the scale developed by Fribourg et al. (2003) was conducted by Basım and Çetin (2011). The 33-item scale consists of six sub-dimensions: "Self-Perception", "Future Perception", "Structural Form", "Social Competence", "Family Cohesion" and "Social Resources".
six months after implementation of the intervention
Study Arms (2)
intervention
EXPERIMENTALNarrative group counseling consists of 8 sessions and will be applied to the intervention group by the researcher.
Control
ACTIVE COMPARATORFor the control group, 4 sessions stress coping interviews will be held after the information meeting, apart from the students' routine practices.
Interventions
Two of the principles that explain how narrative therapy works are: to always maintain a stance of curiosity on the part of the practitioner and to ask questions to which the practitioner does not actually know the answers and to which the answer is known to the participants. To guide therapeutic conversations that include these questions, Michael White and David Epston have designed a series of conversation maps in the application of narrative therapy. Taking these maps into consideration, the sessions were planned with the guidance of relevant literature and structured with expert opinions. Group counseling was applied to the intervention group once a week in 8 sessions. The intervention was completed face to face, in a calm, quiet and bright environment, with a round seating plan. One session lasted 90 minutes. Each session was completed in two parts with a 10-minute break.
In addition to the students' routine practices, four sessions of stress coping interviews will be held for the control group, with an interval of two weeks, after the information meeting.
Eligibility Criteria
You may qualify if:
- Volunteering to participate in the research
- Being 18 years of age or older
You may not qualify if:
- Having a neurological or psychiatric diagnosis based on self-report
- Having attended another similar program, individually or with a group.
- Having attended another similar program, individually or with a group, for at least 1 year ago.
- Being a foreign student.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Gazi Universitylead
Study Sites (1)
Gazi University
Ankara, Çankaya, 06530, Turkey (Türkiye)
Study Officials
- STUDY DIRECTOR
SULTAN AYAZ ALKAYA, Prof.Dr.
Gazi University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- An intervention was applied to both groups and blinding of the participants was ensured. It is planned to analyze the data by a statistician independent of the research. In the study, blinding was not possible since it was the researcher who implemented the intervention.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
November 14, 2023
First Posted
November 18, 2023
Study Start
November 13, 2023
Primary Completion
January 8, 2024
Study Completion
July 1, 2024
Last Updated
July 15, 2024
Record last verified: 2024-07