Skip to content

Effect of Acceptance and Commitment Therapy on Psychotic Severity

Efficacy of Acceptance and Commitment Therapy on Psychotic Severity Among Inpatients With Primary Psychosis: A Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06160869
Enrollment
76
Registered
2023-12-07
Start date
2023-10-01
Completion date
2023-12-20
Last updated
2023-12-07

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

Conditions

Emotion Regulation, Psychosis, Recovery

Keywords

Psychosis, Emotional regulation, Recovery

Brief summary

Our study aims to assess the efficacy of Acceptance and Commitment Therapy on psychotic severity among Inpatients with primary psychosis: A Randomized Controlled Trial.

Detailed description

Current study was an open label, two-arm, parallel, randomized controlled trial, evaluating the efficiency of Acceptance and Commitment Therapy (ACT) added to treatment as usual (TAU) as opposed to treatment as usual (TAU) alone on patients with schizophrenia. The study adheres to the rules for writing Clinical Trials: The Consolidated Standards of Reporting Trials (CONSORT) statement

Interventions

BEHAVIORALAcceptance and commitment therapy

The psychoeducational intervention will consist of seven structured sessions aimed at introducing patients with primary psychosis to the principles and practices of Acceptance and Commitment Therapy (ACT). The primary focus of the intervention is to empower participants to effectively manage distressing thoughts and feelings while pursuing meaningful and valued life goals. Each session covers specific aspects of ACT. Acceptance and commitment therapy will be adminitered in addition to treament as usual provided to patients.

COMBINATION_PRODUCTTreatment as usual

The treatment as usual (TAU) for all patients regardless of condition will consist of hospital treatment, including daily medication management sessions with a psychiatrist (e.g., antipsychotic and other medications as appropriate), community meetings, other group therapy, case management, occupational therapy, open air walks, discharge planning, physical examination, and other services (e.g., medical testing).

Sponsors

Port Said University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

Information is not withheld from trial participants

Intervention model description

Current study is an open label, two-arm, parallel, randomized controlled trial, evaluating the efficiency of Acceptance and Commitment Therapy (ACT) added to treatment as usual (TAU) as opposed to treatment as usual (TAU) alone on patients with schizophrenia. The study adheres to the rules for writing Clinical Trials: The Consolidated Standards of Reporting Trials (CONSORT) statement

Eligibility

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

Inclusion criteria

Participants' criteria of inclusion involved those patients who were 1. Current psychiatric hospitalization; 2. DSM-5 diagnosis of a primary psychotic disorder; (schizophrenia, schizoaffective disorder, delusional disorder, schizophreniform disorder, brief psychotic disorder, and unspecified psychotic disorder, this diagnosis was confirmed by a psychiatrist 3. 18 years or older; 4. ability to talk, read and write in Arabic; and 5. willingness to participate in the study that was scheduled for seven weeks.

Exclusion criteria

Patients were excluded if they 1. had a comorbid learning disability or organic brain disorder; 2. psychosis related to a general medical condition or substance-induced psychotic disorder; 3. were considered mentally unstable; or 4. unfit to participate in the study by their therapist, and/or had newly had (been receiving) psycho-education or somewhat designed psychosocial intervention.

Design outcomes

Primary

MeasureTime frameDescription
Positive and Negative Syndrome Scale (PANSS)7 weeksMeasuring symptom severity of patients with schizophrenia. This is a 30-item instrument. Rating of each item is from (one, no evidence) to (seven, strong evidence) and the total score for overall psychopathology ranges from 30 to 210.

Secondary

MeasureTime frameDescription
Difficulties in Emotion Regulation Scale7 weeksA 36 item measure assesses individuals' typical levels of difficulties in emotion regulation
Recovery Assessment Scale7 weeks38 items scale evaluate mental health recovery

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026