MedPath

Psychological Treatment in Psychiatric Inpatient Care

Not Applicable
Terminated
Conditions
Psychosis
Psychiatric Hospitalization
Compulsory Psychiatric Care Act
Acceptance & Commitment Therapy
Psychiatric Disorder
Registration Number
NCT06012981
Lead Sponsor
Uppsala University
Brief Summary

This study aims to investigate the effect of a brief psychotherapeutic treatment intervention based on ACT, aimed specifically at the vulnerable group of patients in psychiatric 24-hour care treated according to LPT. The study aims to investigate whether a brief number of therapeutic sessions according to ACT during inpatient care produce positive effects on personally relevant life areas for a diagnostically mixed group of patients in a psychiatric intensive care unit.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
1
Inclusion Criteria
  • 18 years old or older.
  • Treated according to the compulsory psychiatric care act.
  • Meet the criterion of informed consent.
Exclusion Criteria
  • Lack the cognitive ability to acquire the treatment intervention, such as impaired attention, memory, logic and reasoning, and also auditory and visual processing. This will be based on a clinical assessment by the ward team, including the attending psychiatrist and a clinical psychologist.
  • Ongoing psychological treatment parallel to the admission.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Change in Bull's Eye Values SurveyFour times daily, from point of inclusion to after a minimum of five data points (approximately a day and a half) after last treatment session

The score ranges from 0-28, higher scores corresponding to better outcome.

Change in GAD-7Four times daily, from point of inclusion to after a minimum of five data points (approximately a day and a half) after last treatment session

The score ranges from 0-21, higher scores corresponding to worse outcome.

Change in Psy-flexFour times daily, from point of inclusion to after a minimum of five data points (approximately a day and a half) after last treatment session

The score ranges from 6-30, higher scores corresponding to better outcome.

Change in Personal QuestionnaireFour times daily, from point of inclusion to after a minimum of five data points (approximately a day and a half) after last treatment session

Scores range from 1-4 per item (number of items might differ between patients as the measure is individually constructed. Higher scores correspond to worse outcome.

Change in PHQ-9Four times daily, from point of inclusion to after a minimum of five data points (approximately a day and a half) after last treatment session

The score ranges from 0-27, higher scores corresponding to worse outcome.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hospital of Västmanland, Västerås

🇸🇪

Västerås, Västmanland, Sweden

Hospital of Västmanland, Västerås
🇸🇪Västerås, Västmanland, Sweden

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.