The Effect of Psychoeducation Program on Healthy Living Behaviors

NCT ID: NCT05208021

Last Updated: 2022-02-10

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

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

52 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-29

Study Completion Date

2022-04-30

Brief Summary

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1.031 / 5.000 Çeviri sonuçları This research was planned to determine the effect of health protection and promotion program based on motivational interviewing based on Pender's Health Promotion Model on healthy lifestyle behaviors of individuals with schizophrenia. When the national and international literature is examined, it is known that there are descriptive studies on the physical health of individuals with mental disorders, and interventional intervention programs under the leadership of psychiatric nurses for the protection and development of the physical health of individuals with mental disorders are very limited. In this context, psychiatric nurses act as a bridge between mental and physical health for patients. It is thought that this study, which will be conducted to evaluate the healthy lifestyle behaviors of individuals with schizophrenia, of the Health Promotion Model and motivational interview-based health protection and promotion program will contribute to the literature, provide data for future studies, and be an applicable model for TRSMs.

Detailed Description

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Research Istanbul Bakirkoy Prof. Dr. In Mazhar Osman Mental Health and Neurological Diseases Training and Research Hospital Bakırköy Community Mental Health Center, the experimental research design was carried out with a pretest and posttest control group. The study population of this study consisted of patients aged 18-65 years who were diagnosed with schizophrenia and other psychotic disorders (N=502). The sample of the study consisted of patients diagnosed with schizophrenia and other psychotic disorders who met the sampling criteria determined in the study (n=52). In the Power analysis of the research, the sample size was determined as 2 groups, with 26 people as the experimental group and 26 people as the control group, with a total of 52 people in the 95% confidence interval. In the study, 52 patients diagnosed with schizophrenia and other psychotic disorders who met the sample selection criteria and volunteered to participate in the study were divided into experimental and control groups using simple random sampling technique. As data collection tools in the research; Personal Information Form, Healthy Life Style Behavior Scale II, Health Improvement Profile, Anthropometric Measurements and Vital Findings and Stage of Change Diagnosis Form were used. The implementation of the research was completed in four stages. In the first stage, the "Health Promotion Model and Motivational Interview-Based Health Protection and Promotion Program" was developed by the researcher in line with the literature review. In the second stage, after the program was introduced to all participants who met the inclusion criteria and their written consent was obtained, pre-tests including the variables of the research were applied, and then the participants were assigned to the experimental and control groups by randomization method. Sessions were held in the form of individual interviews due to the pandemic and social distance conditions. In the third stage, the Health Promotion Model and the Motivational Interview-Based Health Protection and Promotion Program were applied to the experimental group, which consisted of 6 sessions and lasted an average of 60-120 minutes to discuss the warm-up period and the main themes of the sessions in each individual session. A summary of the previous session was made to remember what was done in the first 5-10 minutes of each session. "Weekly Nutrition Follow-up Form", "Weekly Step Count Follow-up Form", "Weekly Stress Follow-up Form", "Weekly Leisure Activities Follow-Up Form" and "Weekly Sleep Diary" prepared by the researcher for the experimental group participants were handed over to the patients as homework. They were asked to fill it out weekly and bring it to their next session. No intervention was made to the patients in the control group during the six-week period. During this process, both experimental and control group patients continued their routine treatments including drug treatments, doctor's controls, psychoeducation, individual therapy, and other programs at the Community Mental Health Center. At the end of the sixth session, the measurement tools were applied again and the implementation phase of the research was ended. After the Health Promotion Model and Motivational Interview-Based Health Protection and Improvement Program sessions applied to the experimental group were completed, the post-test was applied three and six months later, and the control group was followed-up by applying the post-test six weeks, three and six months later.

Conditions

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Schizophrenia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Intervention and control group
Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants
Experimental: Intervention group "Health Promotion Model and the Motivational Interview-Based Health Protection and Promotion Program was applied to the intervention group No Intervention: Control Group Only data collection was carried out. No attempt was made by the researcher during the study

Study Groups

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Intervention group

"Health Promotion Model and the Motivational Interview-Based Health Protection and Promotion Program was applied to the intervention group

Group Type EXPERIMENTAL

Intervention group (Motivational Interviewing)

Intervention Type BEHAVIORAL

The Health Promotion Model and the Motivational Interview-Based Health Protection and Promotion Program were applied to the experimental group, which consisted of 6 sessions and lasted an average of 60-120 minutes. Sessions were held in the form of individual interviews due to the pandemic and social distance conditions.

Control Group

Only data collection was carried out. No attempt was made by the researcher during the study

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Intervention group (Motivational Interviewing)

The Health Promotion Model and the Motivational Interview-Based Health Protection and Promotion Program were applied to the experimental group, which consisted of 6 sessions and lasted an average of 60-120 minutes. Sessions were held in the form of individual interviews due to the pandemic and social distance conditions.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Who agrees to participate in the research himself or his guardian,
* Diagnosed with schizophrenia and other psychotic disorders for at least six months according to DSM-V diagnostic criteria,
* Registered with the Community Mental Health Center and coming regularly,
* Between the ages of 18-65,
* Who can read and write Turkish,
* Using antipsychotic medication for at least six months,
* Not in the "pre-thinking" stage in the change cycle stage,
* No skeletal, muscular, nervous system disease that prevents physical activity or healthy eating,
* They are patients without mental retardation, neurocognitive disorder, alcohol or substance abuse.

Exclusion Criteria

* Failure of himself or his guardian to participate in the research,
* Without a diagnosis of schizophrenia and other psychotic disorders,
* Not coming regularly to the Community Mental Health Center,
* Under 18 years old and over 65 years old,
* Does not speak Turkish,
* Not using regular antipsychotic medication,
* In the "pre-thinking" stage of the cycle of change,
* Those with skeletal, muscular, nervous system diseases that prevent physical activity or healthy nutrition,
* They are patients with mental retardation, neurocognitive disorder, alcohol and substance addiction.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Saglik Bilimleri Universitesi

OTHER

Sponsor Role lead

Responsible Party

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Mahinur Betül Çalışkan

PhD student in nursing departman

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mahinur Betül ÇALIŞKAN, MSc

Role: PRINCIPAL_INVESTIGATOR

Istanbul Saglik Bilimleri University

Locations

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Saglik Bilimleri Universitesi

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Mahinur Betül ÇALIŞKAN, MSc

Role: CONTACT

+05070497185

Melike DİŞSİZ, Assoc. Prof.

Role: CONTACT

+05437995143

Facility Contacts

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Mahinur Betül Çalışkan, MsN

Role: primary

+905070497185

Other Identifiers

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SY200217B08

Identifier Type: -

Identifier Source: org_study_id

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