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Improving Social Climate in Secure Settings With a Compassion Focused Staff Intervention

U

University Psychiatric Clinics Basel

Status

Active, not recruiting

Conditions

Workplace Wellbeing
Compassion
Critical Incident
Social Climate
Staff Support

Treatments

Behavioral: Compassion Focused Staff Support
Behavioral: CFT Workshop

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT07135518
ID ClimACT CFSS

Details and patient eligibility

About

This study evaluates the effectiveness of a Compassion Focused Staff Support (CFSS) intervention in improving the social climate of correctional and forensic psychiatric institutions. The intervention is based on Compassion Focused Therapy and designed to support staff in managing stress, enhancing affect regulation, and strengthening compassion toward self and others. Three institutional units are included in the study. One unit is randomly selected to receive the full CFSS intervention, including a half-day introductory workshop and monthly staff support sessions over six months. A second unit serves as a control group and receives no intervention. A third unit receives only the initial workshop without follow-up sessions. The effect of the intervention is evaluated using a pre-test/post-test design. Outcomes include changes in staff-reported and client-reported social climate, assessed with validated questionnaires, as well as institutional data on critical incidents. The study aims to improve working conditions in secure settings and foster more compassionate, effective staff-client interactions.

Enrollment

52 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Staff Participants:

  • Employed at one of the participating correctional or forensic psychiatric units
  • Aged 18 years or older
  • Willing to provide informed consent

Client Participants:

  • Residing in one of the participating correctional or forensic psychiatric units at the time of data collection.
  • Aged 18 years or older.
  • Capable of providing informed consent

Exclusion criteria

Staff Participants:

  • None (all eligible staff are invited to participate)

Client Participants:

  • Not capable of providing informed consent (e.g., due to acute psychiatric crisis or cognitive impairment).
  • Not deemed competent to participate by treatment team.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

52 participants in 3 patient groups

Intervention
Experimental group
Description:
Full CFSS Group (Workshop + Monthly Groups)
Treatment:
Behavioral: Compassion Focused Staff Support
Partial
Other group
Description:
Workshop-Only Group
Treatment:
Behavioral: CFT Workshop
Control
No Intervention group
Description:
No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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