Narrative Group Counseling and Psychological Resilience

NCT ID: NCT06139068

Last Updated: 2024-07-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-13

Study Completion Date

2024-07-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The intervention group received eight sessions of narrative group counseling. The control group also received four session of stress management training.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Psychological Resilience

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The research was used parallel group, randomized, controlled experimental design.
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

DOUBLE

Participants Outcome Assessors
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.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

intervention

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

Group Type EXPERIMENTAL

Narrative Group Counseling

Intervention Type OTHER

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.

Control

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

Group Type ACTIVE_COMPARATOR

stress coping interviews

Intervention Type OTHER

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.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Narrative Group Counseling

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 Type OTHER

stress coping interviews

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.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Volunteering to participate in the research
* Being 18 years of age or older

Exclusion Criteria

* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Gazi University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Sultan Ayaz Alkaya

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

SULTAN AYAZ ALKAYA, Prof.Dr.

Role: STUDY_DIRECTOR

Gazi University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Gazi University

Ankara, Çankaya, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2023-208536434

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.