Home Treatment for Acute Psychiatric Care

June 3, 2018 updated by: Niklaus Stulz, Psychiatric Services Aargau AG

Home Treatment for Acute Psychiatric Care in the Canton of Aargau (Switzerland): A Randomized Controlled Trial

This study aims to evaluate whether psychiatric home treatment is an effective and efficient alternative to acute inpatient care in mental hospitals. A one-year prevalence cohort of psychiatric patients in need of hospitalization are randomly assigned to either treatment at inpatient wards (treatment as usual) or a new care model with the additional option of treating patients at their homes by mobile care teams. The primary focus is on checking whether optional home treatment leads to a reduction of inpatient days during a two-year follow-up period. In addition, the two service models will be compared regarding treatment cost and outcomes as well as satisfaction of patients and their relatives with psychiatric care.

Furthermore, a sub-cohort of randomly chosen patients from the prevalence-cohort will be examined by a highly trained clinical assessor to test and verify the diagnoses and the clinical ratings made by the staff members of the mental hospital under routine everyday conditions.

Study Overview

Status

Completed

Conditions

Detailed Description

This study aims to evaluate whether psychiatric home treatment is an effective and efficient alternative to acute inpatient care in mental hospitals. A one-year prevalence cohort of psychiatric patients in need of hospitalization are randomly assigned to either treatment at inpatient wards (treatment as usual) or a new care model with the additional option of treating patients at their homes by mobile care teams. The primary focus is on checking whether optional home treatment for crisis intervention leads to a reduction of inpatient days during a two-year follow-up period. In addition, the two service models will be compared regarding treatment cost and outcomes as well as satisfaction of patients and their relatives with psychiatric care.

Furthermore, a sub-cohort of randomly chosen patients from the prevalence-cohort will be examined by a highly trained clinical assessor to test and verify the diagnoses (SCID-I and SCID-II) and the clinical ratings (HoNOS) made by the staff members of the mental hospital under routine everyday conditions.

Study Type

Interventional

Enrollment (Actual)

707

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Aargau
      • Brugg, Aargau, Switzerland, 5201
        • Psychiatric Services Aargau AG

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 64 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Need for acute psychiatric inpatient care
  • Residence in the canton of Aargau
  • Living within 30 minutes (by car) from the headquarters of the home treatment team
  • Health insurance with tarifsuisse

Exclusion Criteria:

  • Insufficient proficiency in German
  • Main diagnosis F0 or F1 (ICD-10)
  • Patients of the forencic departement
  • Patients of the child and adolescent department

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: HEALTH_SERVICES_RESEARCH
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Home treatment
Patients in need of acute psychiatric inpatient care are treated at their houses by mobile treatment teams instead of treatment at mental hospitals whenever home treatment is possible and appropriate.
Patients are treated at home whenever possible and appropriate
ACTIVE_COMPARATOR: Treatment as usual
Patients in need of acute psychiatric inpatient care are treated at a mental hospital.
Patients are treated at a mental hospital

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of inpatient days
Time Frame: 2 years follow-up
2 years follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total days in treatment (inpatient + home treatment)
Time Frame: 2 years follow-up
2 years follow-up
Direct treatment costs
Time Frame: 2 years follow-up
2 years follow-up
Health of the Nation Outcome Scales (HoNOS)
Time Frame: Intake and discharge from treatment episode (expected average of 4 weeks)
Participants will be followed for the duration of hospital stay, an expected average of 4 weeks.
Intake and discharge from treatment episode (expected average of 4 weeks)
Brief Symptom Checklist (BSCL)
Time Frame: Intake and discharge from treatment episode (expected average of 4 weeks)
Participants will be followed for the duration of hospital stay, an expected average of 4 weeks.
Intake and discharge from treatment episode (expected average of 4 weeks)
Perceptions of Care-18
Time Frame: Discharge from treatment episode (expected average of 4 weeks)
Participants will be assessed at discharge from hospital, after an expected average of 4 weeks.
Discharge from treatment episode (expected average of 4 weeks)
Satisfaction of patients' relatives
Time Frame: Discharge from treatment episode (expected average of 4 weeks)
Relatives' satisfaction will be assessed with an adapted version of the Perceptions of Care-18 questionnaire at discharge of the patients from hospital, after an expected average of 4 weeks. The proportion of satisfied relatives will be reported for both study arms.
Discharge from treatment episode (expected average of 4 weeks)
Number of rehospitalizations per patient
Time Frame: 2 years follow-up
2 years follow-up
Number of patients with adverse events
Time Frame: 2 years follow-up
E.g. suicide or attempted suicide.
2 years follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Niklaus Stulz, PhD, Psychiatric Services Aargau AG

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 1, 2015

Primary Completion (ACTUAL)

April 1, 2018

Study Completion (ACTUAL)

April 1, 2018

Study Registration Dates

First Submitted

December 11, 2014

First Submitted That Met QC Criteria

December 22, 2014

First Posted (ESTIMATE)

December 23, 2014

Study Record Updates

Last Update Posted (ACTUAL)

June 6, 2018

Last Update Submitted That Met QC Criteria

June 3, 2018

Last Verified

June 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PDAG-0001

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Mental Disorders

Clinical Trials on Home treatment

Subscribe