A Psychoeducational Intervention for Brain Awareness, Metacognition, Self-efficacy and Treatment Motivation

NCT ID: NCT05812469

Last Updated: 2023-04-13

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

COMPLETED

Clinical Phase

NA

Total Enrollment

77 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-01

Study Completion Date

2023-03-01

Brief Summary

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The aim of this study is to examine the effect of brain awareness intervention on metacognition, self-efficacy and treatment motivation in patients with alcohol and substance use disorders. It is an experimentally designed study with a randomized control group and repeated measurements (pre-test, mid-test, post-test).

Detailed Description

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The aim of this study is to examine the effect of brain awareness intervention on metacognition, self-efficacy and treatment motivation in patients with alcohol and substance use disorders. It is an experimentally designed study with a randomized control group and repeated measurements (pre-test, mid-test, post-test). 77 inpatients at the Alcohol and Drug Addiction Treatment and Research Center included between April and October 2021. In addition to standard treatment, psychoeducation and counseling provided as part of the Brain Awareness Intervention for the experimental group of 39 patients. The control group of 38 patients will receive education about Being Healthy in addition to standard treatment and standard follow-up. Patients' pathological metacognitive activities, self-efficacy perceptions and treatment motivation will assessed with the Metacognition Scale-30, Self-Efficacy Scale and Treatment Motivation Questionnaire using one-way and two-way repeated measures analysis.

Conditions

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Substance Use Disorders Alcohol Use Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

It is an experimentally designed study with a randomized control group and repeated measurements (pre-test, mid-test, post-test).
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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experimental group

psychoeducation and counseling provided as part of the Brain Awareness Intervention for the experimental group of 39 patients

Group Type EXPERIMENTAL

Brain Awareness Intervention

Intervention Type BEHAVIORAL

effect of brain awareness intervention on metacognition, self-efficacy and treatment motivation in patients with alcohol and substance use disorders

control group

38 patients will receive education about Being Healthy

Group Type ACTIVE_COMPARATOR

Being Healthy Education

Intervention Type BEHAVIORAL

This training included trainings on Healthy Nutrition, Sexually Transmitted Diseases, Importance of Physical Activity and Personal Hygiene prepared by the researcher in the form of presentations for the patients in the control group.

Interventions

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Brain Awareness Intervention

effect of brain awareness intervention on metacognition, self-efficacy and treatment motivation in patients with alcohol and substance use disorders

Intervention Type BEHAVIORAL

Being Healthy Education

This training included trainings on Healthy Nutrition, Sexually Transmitted Diseases, Importance of Physical Activity and Personal Hygiene prepared by the researcher in the form of presentations for the patients in the control group.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Being between the ages of 18-65 and able to read and write
2. Inpatient treatment with alcohol or substance abuse problem
3. To not have a psychiatric (severe depression, bipolar disorder or psychosis) or mental illness that would prevent participation in the study

Exclusion Criteria

1. Failure to participate in more than one session despite agreeing to participate in the research
2. Taking the decision to terminate treatment or early discharge by violating treatment rules during the treatment process
3. Not participating in post-discharge follow-up or post-test application
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

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Halil İbrahim ÖLÇÜM

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Halil Ibrahim Olcum

Çorum, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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BA-project

Identifier Type: -

Identifier Source: org_study_id

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