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Experiences and impact of coercive measures in Mental Health Care.

Experiences and impact of coercive measures in Mental Health Care. - Coercive measures and trauma.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43847
Enrollment
318
Registered
2016-10-24
Start date
2014-02-04
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychotrauma PTSD

Interventions

Coercive measures
Experiences
Trauma

Sponsors

Parnassia Bavo Groep (Den Haag)
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Admitted patients of closed acute admission ward in a psychiatric hospital Patients who experienced one of the test coercive measure during admission Crisis is in remission Age above 18 Good skills in reading an speaking dutch

Exclusion criteria

Exclusion criteria: Patients who don't understand the Dutch language Patients who are unable to participate in the study due to their mental state

Design outcomes

Primary

MeasureTime frame
Primary study parameters are the experiences with regard to coercive measures, the frequency and intensity of PTSD symptoms during recording and three months after discharge and coping strategies.

Secondary

MeasureTime frame
The following background variables are mapped: * Gender * Age * Ethnicity * Main diagnosis * Severity psychopathology (K Axis) * Type coercive measure * Previous coercion experience * Events during current admission (PEQ) * Positive experience during current admission * Duration admission * Subscales Coercion Experience Scale (CES) * Subscales coping strategies (DUBRICSI) Possible selection bias will be mapped through an inventory of characteristics of non-participating patients. These are: the reason for not being able / willing to take part in the survey, the main diagnosis, gender, age, admission time and the reason for admission.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)