Evaluation of Psychotherapeutic Intervention Model in Nursing

NCT ID: NCT06076746

Last Updated: 2025-05-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-14
• Study Completion Date: 2024-12-27

Brief Summary

This study aims to evaluate the efficacy of a psychotherapeutic intervention model in nursing on the nursing diagnosis ineffective coping. For this purpose, validity and reliability studies of the assessment tools will be carried out initially, and then a randomized controlled study will be conducted.

Detailed Description

This study aims to evaluate the efficacy of the psychotherapeutic intervention model in nursing on patients with nursing diagnosis of ineffective coping (International Classification of Nursing Practices (ICNP)/North American Nursing Diagnostic Association (NANDA)). For this purpose, first of all, validity and reliability studies of "Coping" and "Self-Esteem", which are the results of NOC (Nursing Outcomes Classification), will be conducted, and then a randomized controlled study will be conducted (Turkish version). 200 patients will be included in the validity and reliability phase of the study, which was conducted in a hospital outpatient psychiatric setting in Turkey. The randomized controlled second phase will be carried out, single-blind, nurse-led, with approximately 20 patients with anxiety randomized to intervention (n=10) or control groups (n=10). The usual treatment and care will be compared with the application of the psychotherapeutic intervention model previously developed in nursing.

Conditions

Anxiety Generalized

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Experimental: Intervention(s) for ineffective coping in General Anxiety

Patients with nurse diagnosis of ineffective coping will be treated using Nursing Interventions Classification (NIC) psychotherapeutic intervention(s).

Group Type: EXPERIMENTAL

NIC Psychotherapeutic Intervention(s) for İneffective Coping

Intervention Type: BEHAVIORAL

Patients will be treated by NIC psychotherapeutic intervention(s) for general anxiety (e.g. anxiety reduction, coping enhancement).

psychotherapeutic intervention

Intervention Type: BEHAVIORAL

Patients will be treated by NIC psychotherapeutic intervention(s) for general anxiety (e.g. anxiety reduction, coping enhancement).

Treatment-as-Usual for General Anxiety

Patients with nurse diagnosis of ineffective coping will receive the usual treatment for general anxiety.

Group Type: ACTIVE_COMPARATOR

psychotherapeutic intervention

Intervention Type: BEHAVIORAL

Patients will be treated by NIC psychotherapeutic intervention(s) for general anxiety (e.g. anxiety reduction, coping enhancement).

Interventions

NIC Psychotherapeutic Intervention(s) for İneffective Coping

Patients will be treated by NIC psychotherapeutic intervention(s) for general anxiety (e.g. anxiety reduction, coping enhancement).

Intervention Type: BEHAVIORAL

psychotherapeutic intervention

Patients will be treated by NIC psychotherapeutic intervention(s) for general anxiety (e.g. anxiety reduction, coping enhancement).

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• 18-64 years old,
• Literacy,
• Having applied to the psychiatry outpatient clinic,
• Being regularly treated in a psychiatry outpatient clinic,
• Having a medical diagnosis of generalized anxiety disorder,
• Having at least one of the defining characteristics of the nursing diagnosis of ineffective coping according to the nursing process.

Exclusion Criteria

• Medical diagnosis of dementia or psychotic spectrum disorder,
• Cognitive disorder,
• Confused state of consciousness
• Psychomotor agitation,
• Moderate or severe intellectual disability
• Expressing suicidal thoughts
• Suicide attempt in the last month
• Continuing psychological counseling at the moment.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tuğba Aşkan

OTHER

Sponsor Role: lead

Responsible Party

Tuğba Aşkan

Nurse

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Tuğba Aşkan, PhD Student

Role: PRINCIPAL_INVESTIGATOR

Ankara Yildirim Beyazıt University

Locations

Ankara Yildirim Beyazit University

Ankara, Çubuk, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

2022-1081

Identifier Type: -

Identifier Source: org_study_id