Fact CheckerSign in

NCT07310615Completed

Mindfulness Psychoeducation for Schizophrenia

Mindfulness-Based Psychoeducation Improves Mindfulness and Medication Adherence in Schizophrenia: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 30 Dec 2025

Brief summary (registry, in English)

This study aims to examine the effects of a mindfulness-based psychoeducation program on mindfulness levels and treatment adherence among individuals diagnosed with schizophrenia. Schizophrenia is a chronic psychiatric disorder that affects thinking, emotions, and behavior, and difficulties in adhering to prescribed treatments are commonly observed. Poor treatment adherence is associated with relapse, increased hospitalization, and reduced overall functioning. This randomized controlled study includes 40 patients assigned to either an experimental group or a control group. The experimental group receives a structured mindfulness-based psychoeducation program, while the control group receives treatment as usual without any additional intervention. Assessments are conducted before and after the intervention using a Personal Information Form, a Mindfulness Scale, and the Morisky Medication Adherence Scale.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
9 Dec 2025
Start date
25 Dec 2024
Primary completion date
13 Jul 2025
Lead sponsor
Ömer USLU
NCT number
NCT07310615

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 25 Dec 2024 to the primary completion date, 13 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Comorbid intellectual disability, neurological disorder, or severe cognitive impairment
  • Severe visual or hearing impairment preventing participation
  • Any condition judged by the clinician to contraindicate participation in group sessions

Other

  • Presence of acute psychotic symptoms requiring immediate hospitalization
  • Substance or alcohol dependence within the last 6 months
  • Participation in any mindfulness-based or psychoeducational program within the last year

Who the study is looking for

  • Diagnosis of schizophrenia according to DSM-5 criteria
  • Age between 18-65 years
  • Being clinically stable for at least the past 3 months
  • Able to communicate, read, and understand Turkish
  • Receiving outpatient psychiatric follow-up
  • Willingness to participate and providing informed consent

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Söke Fehime Faik Kocagöz State Hospital
Coordinator of this site? Confirm its status
AydinTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.