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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03140618
Other study ID # 3500LJUSMILJO
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 15, 2017
Est. completion date December 31, 2020

Study information

Verified date October 2021
Source Umeå University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The care environment influences both patients' experiences of care as well as staff's experiences of the work environment. A radical change in physical environment is planned at a psychiatric ward, aiming at creating a care environment that supports patients' opportunities for recovery from mental ill-health and to create a better and more attractive work environment for the staff. The rebuilding involves a new ward layout and new innovations such as light installations, a comfort room and an activity room. The study uses a single-system design to evaluate the effects of the intervention - the rebuilt ward. Both quantitative and qualitative data will be used in the evaluation. Data will be collected using questionnaires measuring dimensions of patients' well-being and experiences of the care environment, staff's experiences of work-related stress and work environment, quality of care, a device measuring physical activity, existing clinical registers and data from medical files, staff' sick leave, participant observations, and semi-structured interviews. This evaluation study, to our knowledge the first of it's kind in Sweden, is expected to generate important knowledge of the effect of the change process that can be used at other psychiatric wards to design the inpatient care environment. In the long run, the study could lead to a better reputation of psychiatric nursing and to more attractive workplaces.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 67 Years
Eligibility Inclusion Criteria for Patients - 18 years or older - Admitted to the wards during either A phase, B phase and/or follow-up Exclusion Criteria for Patients - Does not master the Swedish language well enough to complete questionnaires and participate in interviews Inclusion Criteria for Staff: - Regularly employed at the ward during A and B phase and/or follow-up. Exclusion Criteria for Staff: - Staff employed by the hour

Study Design


Related Conditions & MeSH terms


Intervention

Other:
The light and environment project in psychiatric inpatient care
Complete rebuilding of a hospital ward. The ward layout is remodeled and different devices and services are installed such as light, sound, and color settings, increased opportunities for physical activity, social harmony, privacy, peace, and quiet. A comfort room and a activity room will be built.

Locations

Country Name City State
Sweden Umeå university Umeå

Sponsors (2)

Lead Sponsor Collaborator
Umeå University Västerbotten County Council, Sweden

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Outcome Rating Scale [patients] The Outcome Rating Scale measures self-assessed satisfaction with life on four visual-analogue scales. Changes during baseline and intervention period (measured regularly for 12 weeks)
Primary Perceived stress [staff] PSS consists of 10 items answered on a 5-point Likert scale Changes during baseline and intervention period (measured regularly for 12 weeks)
Secondary Quality of interactions [patients] This is measured using The Caring Professional Scale (CPS) that consists of 14 items answered on a 5-point Likert scale. Changes during baseline and intervention period (measured regularly for 12 weeks)
Secondary Anxiety and depressive symptoms [patients] The Hospital Anxiety and Depression Scale (HAD) will be used to measure anxiety and depressive symptoms. All items are scored on a 4-point scale. Changes during baseline and intervention period (measured regularly for 12 weeks)
Secondary Quality in psychiatric care [patients] The QPC-IP measures quality of care on 30 items using a 4-point scale. Changes during baseline and intervention period (measured regularly for 12 weeks)
Secondary Stress of Conscience [staff] The Stress of Conscience Questionnaire (SCQ) will be used to measure the frequencies of stressful situations and the degree to which these lead to stress of conscience among staff. Changes during baseline and intervention period (measured regularly for 12 weeks)
Secondary Quality of care [staff] The Quality in Psychiatric Care- Inpatient Staff (QPC-IPS) questionnaire will be used to measure quality of care. Changes during baseline and intervention period (measured regularly for 12 weeks)
Secondary Physical activity [patients and staff] An electronic device measuring physical activity will be carried by participants during one week before and after rebuilding the ward. Changes in physical activity between baseline and intervention