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Application of a Mindfulness and Self-Compassion Program in Patients With Schizophrenia. Randomized Controlled Trial.

Application of a Mindfulness and Self-Compassion Program in Patients With Schizophrenia. Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04144075
Acronym
ACAMP2020
Enrollment
150
Registered
2019-10-30
Start date
2020-05-01
Completion date
2021-02-15
Last updated
2019-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Keywords

Psychosis, Quality of life, Mindfulness, Compassion, Self-compassion, Schizophrenia

Brief summary

This is a randomized clinical trial to check whether the quality of life of patients with schizophrenia improves after participation in the mindfulness and self-compassion (MSC) programme.

Detailed description

MAIN AIM To check whether the quality of life of patients with schizophrenia improves after participation in the mindfulness and self-compassion (MSC) programme, compared with those participating in an active control programme or those following usual treatment. DESIGN Randomized clinical trial, three parallel groups: 1. Experimental, which will receive the MSC together with the usual treatment (TAU). 2. Active control, which will receive an alternative programme with cognitive, behavioural and psychoeducational components (CBTG) together with the TAU. 3. Passive control, which will receive the TAU. STUDY DISORDER Schizophrenia. DATA FROM THE INTERVENTION UNDER STUDY Program developed by Kristin Neff and Christopher Germer, after observing in diverse investigations the inverse correlation between levels of self-pity and diverse pathological clinical variables. POPULATION UNDER STUDY Patients from Telde's Mental Health Unit who have been diagnosed with schizophrenia. TOTAL NUMBER OF SUBJECTS 150

Interventions

It is a protocolized training program in mindfulness and self-compassion skills. It has a duration of 8 weekly group sessions of about two hours and 45 minutes and a silent retreat of 4 hours.

BEHAVIORALCognitive Behaviour Therapy Group

It is a control intervention designed for the development of a control group suitable for comparison with experimental groups.

OTHERTreatment as usual

It is variable according to the clinical and personal characteristics of the patient, the most common components will be described.

Sponsors

Gutiérrez-Hernández, ME
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of schizohrenia

Exclusion criteria

* Drug addict

Design outcomes

Primary

MeasureTime frameDescription
World Health Organization Quality of Life Instument. WHOQOL-BREF15 minutesScores from 5 to 130, the higher score the worse outcome.

Secondary

MeasureTime frameDescription
Self-compassion scale (SCS)15 minutesScores from 5 to 130, the higher score the worse outcome

Contacts

Primary ContactMaría Elena F Gutiérrez-Hernández
benchara@gmail.com658024211

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026