Managing Patient Aggression in Mental Health Services

Mental Disorders Clinical Trial

— Violin  

Official title:

The Effectiveness of User-driven Intervention to Manage Patient Aggression in Mental Health Services

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02724748
• Other study ID #: 294298
• Status: Completed
• Phase: N/A
• Start date: February 2016
• Est. completion date: December 31, 2018

Study information

• Verified date: February 2020
• Source: University of Turku
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To compare the effects of an educational intervention to usual practice (no specified staff education) on improving treatment culture and supporting team climate in staff members, which further could reduce the need for the use of coercive methods in psychiatric care.

Description:

This is a single-blind, two-arm, cluster randomised controlled trial involving 28 psychiatric hospital wards across Finland.

Units are randomised on an equal basis to receive either staff educational programme (designed together with staff members, patients and relatives on the study units) or standard care. Inpatient psychiatric hospital organisations are the unit of randomisation. The cluster design will be used to avoid contamination between individual staff members in each study ward. We will use centralized randomisation at the University of Turku (Department of Mathematics and Statistics). Randomisation will be fully concealed and computer-generated by an independent statistician, who is not involved in the study. Investigators enrolling wards cannot foresee assignment. Outcome assessors and statisticians will be kept blinded to allocation. However, due to the type of intervention, allocation will be unmasked to patients and their relatives, contact persons in each ward, and health care staff delivering patient care on the wards after randomisation; this would reflect real-world care. While the Data Monitoring Committee undertook ongoing safety surveillance, investigators running the preliminary analysis for the Data Monitoring Committee will be masked to data until investigators released the database. Further, the statisticians and the National Register holder who are responsible in Finnish routine data used in this study, will be masked to ward allocation and patient data in each group. Randomisation will be done after collecting the baseline data from each unit.

Baseline data on coercive practices used on the units will be collected by the members of the research team with a help of staff members within the eight weeks, while observational and interview data related to the quality of the services will be collected by the research team (only in the intervention units). On the individual level, all staff members working in the study units, patients, and their relatives are eligible to participate in the study. Staff survey and interviews with staff members, patient groups and relatives will be done on the basis of free will. The staff of the unit/research team members will approach patients and their relatives to explain the purpose of the study and its arrangements orally and in written format. The opportunity to ask questions about the study will be given to them. Those that will be assessed having a lack of capacity to give informed consent and declined to participate will not be interviewed. Staff surveys will be repeated for baseline and follow-up. On the organisational level, the outcomes related to patient service use will be assessed 12 and 24 months after baseline data collection.

Assessing quality components: The strengths, weaknesses, opportunities, and threats related to the new practices will also be discussed and categorised based on SWOT analysis (Strength, Weakness, Opportunity, Threat). Possible barriers and facilitating factors for change on the on each unit will be identified. The quality of the service facilities will be assessed by observations on the units, based on World Health Organization's (2012) QualityRight Tool Kit focusing on five central quality criteria.

We have systematically searched for, but found no directly relevant past work. We assume that if the data will be obtained from local hospital registers by sampling 7 clusters (hospitals) with 265 subjects each in intervention group and 7 clusters with 265 subjects each in control group, we will have 80% power to detect a difference between the group proportions of -0.0400. The control group proportion is 0.1100. The intervention group proportion is assumed to be 0.1100 under the null hypothesis and 0.0700 under the alternative hypothesis. The test statistic used is the two-sided Z test (unpooled) with an overall significance level at 0.05. We may assume based on the hospital registers that sample size for the total population admitted in the study wards in one year will be 3710. However, if we consider a loss of 20% patients in the local care registers, the total number of patients on the randomised wards should be about 4454 patients. Further, if we assume 50% response rate for patient survey out of possible 3710 participants, we will assume that we will obtain 928 filled questionnaires during 6 month survey data collection period. The sample size calculation was adjusted for intra-cluster correlation at 0.005.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: December 31, 2018
• Est. primary completion date: December 31, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 99 Years

Eligibility

Inclusion Criteria:

• Finnish speaking hospital organisations

• at least 1 psychiatric ward

• open 24/7

• are able to use coersive measures (seclusion room, limb restraint, forced medication, physical restraint)

Exclusion Criteria:

• wards specialised in forensic, psychogeriatric, or child and adolescent care alone

• similar type of project is underway or is planned to start

Related Conditions & MeSH terms

• Aggression
• Mental Disorders

Intervention

Behavioral:
• Educational intervention
Educational intervention for staff members will encourage collaboration between patients, relatives and staff members. Skills, intellectual resources, motivation and encouragement among staff members to make changes on the unit will be supported. More detailed content of the intervention to be used in each unit will be tailored based on preparatory phase of the study and individual needs of the unit. The educational intervention will be carried out beside usual care.

Locations

Country	Name	City	State
n/a

Sponsors (10)

Lead Sponsor	Collaborator
University of Turku	Academy of Finland, Harvard Medical School, Harvard School of Public Health, Sichuan University of China, China, Stanford University, The Hong Kong Polytechnic University, Turku University Hospital, University of Nottingham, World Health Organisation, Philippines

References & Publications (2)

Välimäki M, Yang M, Normand SL, Lorig KR, Anttila M, Lantta T, Pekurinen V, Adams CE. Study protocol for a cluster randomised controlled trial to assess the effectiveness of user-driven intervention to prevent aggressive events in psychiatric services. BMC Psychiatry. 2017 Apr 4;17(1):123. doi: 10.1186/s12888-017-1266-6. — View Citation

Välimäki M, Yang M, Vahlberg T, Lantta T, Pekurinen V, Anttila M, Normand SL. Trends in the use of coercive measures in Finnish psychiatric hospitals: a register analysis of the past two decades. BMC Psychiatry. 2019 Jul 26;19(1):230. doi: 10.1186/s12888- — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The incidence of seclusion room use.	The incidence of seclusion room use by patients in each unit.	Three years
Secondary	Other types of coercive measures	Organisational outcomes. Incidence of other types of coercive measures used on patients (limb restraint, forced injection, physical restraint).	Three years
Secondary	Service use	Organisational outcomes. Type of admission, length of stay, deaths.	Three years
Secondary	Team climate	Staff outcomes. Team Climate Inventory, TCI.	18-20 months after beginning of the intervention
Secondary	Turnover	Staff outcomes.	Three years
Secondary	The functional capacity of patients	Patient outcomes. Gobal Assessment Scale, GAS.	Nine months after beginning of the intervention
Secondary	Patient treatment satisfaction	Patient outcomes. Client Satisfaction Questionnaire, CSQ-8.	Nine months after beginning of the intervention
Secondary	Quality of Life	Patient outcomes. Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form, Q-LES-Q-SF	Nine months after beginning of the intervention

External Links

•   Study protocol
•   Trends