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Clinical Trials/NCT06012981
NCT06012981TerminatedNot Applicable

Psychological Treatment in Psychiatric Inpatient Care

Uppsala University2 sites in 1 country1 target enrollmentStarted: September 1, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
1
Locations
2
Primary Endpoint
Change in Bull's Eye Values Survey

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Outcomes

Primary Outcomes

Change in Bull's Eye Values Survey

Time Frame: Four 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-7

Time Frame: Four 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-flex

Time Frame: Four 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 Questionnaire

Time Frame: Four 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-9

Time Frame: Four 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 Outcomes

No secondary outcomes reported

Investigators

Sponsor
Uppsala University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marten Tyrberg

Principal Investigator

Uppsala University

Study Sites (2)

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