Ireland
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Active, not recruiting Not applicable

TTM-Based Social Media Psychoeducation for Psychosis

NCT07080827 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-03-01
Last updated
2025-07-23

Condition(s) studied

Treatment ComplianceSocial MediaPsychotic Disorders

Investigational drug(s) / intervention(s)

TTM-Based Online Psychoeducation ProgramStandard Face-to-Face Psychoeducation ProgramTTM-Based Online Psychoeducation Program

TTM-Based Online Psychoeducation Program: A 5-week structured psychoeducation program based on the Transtheoretical Model (TTM), delivered via WhatsApp. Educational content was tailored to the participant's stage of change and included videos, texts, and interactive materials to promote treatment adherence in individuals with psychosis.

Standard Face-to-Face Psychoeducation Program: A 3-week conventional psychoeducation program delivered face-to-face at the Community Mental Health Center. The program focused on general treatment adherence without utilizing the Transtheoretical Model and included verbal education, printed materials, and discussions.

TTM-Based Online Psychoeducation Program: The intervention was provided after a 3-month delay following initial observation. Participants received the same 5-week online psychoeducation program as the main intervention group

Study summary

This doctoral research investigates the effect of a Transtheoretical Model (TTM)-based psychoeducation program delivered via social media on treatment adherence in individuals diagnosed with psychosis. The study follows a randomized controlled trial design with pretest, posttest, and three-month follow-up assessments.

A total of 60 participants were selected from among 354 individuals registered at the Balıkesir Community Mental Health Center (CMHC), based on predefined inclusion and exclusion criteria. Participants were randomly assigned into three groups:

1. an online intervention group receiving a 5-week TTM-based treatment adherence psychoeducation program via WhatsApp;
2. a face-to-face intervention group receiving a standard, non-TTM-based treatment adherence psychoeducation program over 3 weeks at the CMHC; and
3. a control group that received no educational intervention, only assessments.

Data collection instruments include a Sociodemographic Information Form, the Stage of Change Identification Form, the Medication Adherence Report Scale (MARS-5), and the Clinical Global Impression-Severity Scale (CGI-S). Measurements were conducted at baseline, post-intervention, and three months after the intervention.

The study hypotheses are:

Research Hypotheses H1: The treatment adherence scale scores of individuals diagnosed with psychosis who participate in the TTM-based psychoeducation group administered via social media will differ compared to the scores of individuals who participate in the face-to-face treatment adherence psychoeducation group.

H2: The treatment adherence scale scores of individuals diagnosed with psychosis who participate in the TTM-based psychoeducation group administered via social media will differ compared to the scores of individuals who do not receive TTM-based psychoeducation.

This study aims to provide evidence for the efficacy of theory-based, technology-supported psychoeducation programs in enhancing treatment adherence among individuals with psychosis. Furthermore, it evaluates whether a model-based online psychoeducation program is more effective than a conventional treatment adherence education.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 18 and 65 years * Diagnosed with a psychotic disorder according to DSM-5 criteria, including: * Schizophrenia * Schizophreniform disorder * Schizoaffective disorder (with mild mood symptoms) * Brief psychotic disorder * Substance/medication-induced psychotic disorder (in remission) * Paranoid disorder * On the same prescribed psychiatric medication for at least one month * Able to communicate in Turkish * Has access to the internet and owns at least one active social media account (Instagram, Twitter, Facebook, WhatsApp, etc.) * Literate and able to complete self-report forms * Willing to participate and provide informed consent * Clinical Global Impression-Severity (CGI-S) score of 4 or below Exclusion Criteria: * Under 18 or over 65 years of age * Acute psychotic episode at the time of recruitment * Comorbid psychiatric diagnoses not covered under the inclusion list * Diagnosed with neurocognitive disorders (e.g., dementia) * Diagnosed with intellectual disability (mental retardation) * Unable to use smartphone, tablet, or other digital communication tools * Missed more than 20% of the intervention sessions

Primary outcome measure(s)

  • Medication Adherence (Treatment adherence) — Baseline (Week 0) and Post-Intervention (Week 5)
    Score on a 5-point Likert scale
  • Change in Medication Adherence Scores (MARS-5) — Baseline, Post-Intervention (Week 5), and 3-Month Follow-Up
    Medication adherence will be assessed using the 5-item Medication Adherence Report Scale (MARS-5), originally developed by Horne and Hankins (2001). It is a generic, self-reported Likert-type scale validated across various chronic physical and psychiatric conditions, including bipolar disorder, hypertension, asthma, and schizophrenia. Each item is rated on a 5-point scale from 1 (always) to 5 (never), yielding a total score between 5 and 25. Higher scores indicate better adherence. The Turkish version of the scale was adapted by the investigators and demonstrated acceptable internal consistency (Cronbach's α = 0.78). Factor analyses supported a unidimensional structure (KMO = 0.79; CFI = 0.97; RMSEA = 0.089), consistent with the original. In this study, MARS-5 will be administered at three time points: prior to the intervention (baseline), immediately following the intervention (post-test), and three months after the intervention (follow-up) to assess changes in treatment adherence

Trial sites (1)

FacilityCityRegionStatus
Balıkesir Provincial Health Directorate, Community Mental Health Center Balıkesir Balıkesir
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07080827 on ClinicalTrials.gov ↗ ← All trials in Turkey