NCT06139068

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
68

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 13, 2023

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

November 14, 2023

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 18, 2023

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 8, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2024

Completed
Last Updated

July 15, 2024

Status Verified

July 1, 2024

Enrollment Period

2 months

First QC Date

November 14, 2023

Last Update Submit

July 12, 2024

Conditions

Keywords

Psychological ResilienceNarrative TherapyNursing StudentsPsychiatric nursing

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

EXPERIMENTAL

Narrative group counseling consists of 8 sessions and will be applied to the intervention group by the researcher.

Other: Narrative Group Counseling

Control

ACTIVE COMPARATOR

For the control group, 4 sessions stress coping interviews will be held after the information meeting, apart from the students' routine practices.

Other: stress coping interviews

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.

intervention

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.

Control

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Gazi University

Ankara, Çankaya, 06530, Turkey (Türkiye)

Location

Study Officials

  • SULTAN AYAZ ALKAYA, Prof.Dr.

    Gazi University

    STUDY DIRECTOR

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
Model Details: The research was used parallel group, randomized, controlled experimental design.
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

Locations