Psychosis Clinical Trial
— PCPCOfficial title:
Person-Centered Psychosis Care: An Educational Intervention for Inpatient Staff
NCT number | NCT03182283 |
Other study ID # | PCPC |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 25, 2014 |
Est. completion date | August 1, 2018 |
Verified date | November 2018 |
Source | Göteborg University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Schizophrenia is a major mental illness that presents in young adulthood and affects ~1% of
the population. Impact on affected persons life is often major and life expectancy is reduced
by ~20 years. Better and more effective care models are needed to increase health in these
persons. Person-centered care have been suggested to be one way to increase efficiency in
care delivery for patients with chronical and complex conditions. The impact of
person-centered care on a inpatient psychosis care setting is now being tested.
The purpose of this study is to test whether inpatient Person-centered psychosis care (PCPC)
can
1. increase patient empowerment
2. improve patient satisfaction
3. reduce the frequency of involuntary treatments
4. reduce the duration of inpatient care and
5. reduce overall ward burden
A further purpose is to qualitatively explore which components in this complex intervention
are experienced as facilitators or barriers to the achievement of good care, from both
patient, next-of-kin and staff perspectives.
Quantitative data is collected through questionnaires from patients (measuring empowerment,
care satisfaction and perceived health) before and after an educational intervention for
staff, along with ward level measures such as care burden, number of involuntary treatments
and length of stay on ward.
Qualitative interview is used to study experiences of patients, next-of-kin and staff.
Status | Completed |
Enrollment | 100 |
Est. completion date | August 1, 2018 |
Est. primary completion date | August 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Diagnosis of psychotic illness in accordance with ICD-10 - Medically ready for discharge as deemed by ward psychiatrist Exclusion Criteria: - Severe cognitive disability - Lack of basic Swedish language skills |
Country | Name | City | State |
---|---|---|---|
Sweden | Psychosis Clinic, Sahlgrenska University Hospital | Göteborg |
Lead Sponsor | Collaborator |
---|---|
Göteborg University | Sahlgrenska University Hospital, Sweden, Swedish Council for Working Life and Social Research |
Sweden,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in patient empowerment (between before and after cohorts) | Patient reported empowerment measured by The Empowerment Scale (Rogers et al 2010). | Baseline (for before-intervention cohort), 2 years (for after-intervention cohort) | |
Secondary | Change in consumer satisfaction (between before and after cohorts) | Patients satisfaction with different aspects of care measured by UKU-ConSat Rating Scale (Ahlfors et al 2000). | Baseline (for before-intervention cohort), 2 years (for after-intervention cohort) | |
Secondary | Change in staff care burden (before and after intervention and implementation) | Overall care burden as reported by staff daily (objective and subjective items) in an internal instrument used by the Psychosis Clinic for quality monitoring. | Baseline, 2 years | |
Secondary | Change in inpatient days with/out involuntary care (between before and after cohorts) | Mean number of inpatient days, mean number of inpatient days with compulsory care. | Baseline (for before-intervention cohort), 2 years (for after-intervention cohort) | |
Secondary | Change in involuntary treatment (between before and after cohorts) | Mean number of involuntary treatment interventions (involuntary injections, medical restraint) | Baseline (for before-intervention cohort), 2 years (for after-intervention cohort) |
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