Skip to content

Feasibility Study to Test the Effectiveness of Open Dialogue Training for Psychiatric Staff

Feasibility Study to Test the Effectiveness of Open Dialogue Training for Psychiatric Staff - single group pre- and post-intervention comparisons - Feasibility Study to Test the Effectiveness of Open Dialogue Training for Psychiatric Staff - single group pre- and post-intervention comparisons

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055266
Enrollment
25
Registered
2024-08-19
Start date
2025-01-29
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

healthy psychiatric professionals

Interventions

Group training once a week, 2 hours per session, for a total of 8 sessions (16 hours total) to become an Open Dialogue practitioner

Sponsors

Keio University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Eligible applicants will be health care professionals who work full-time at Oouchi Hospital and meet the following selection criteria. -Those who are medical professionals (physicians, nurses, mental health workers, licensed psychologists, clinical psychologists, occupational therapists, and physical therapists), and responsible for the care and treatment of psychiatric patients in their daily work. -Those who are currently in good physical condition to work. -Those who are able to participate in all training sessions. -Those who can provide written consent to participate in the study.

Exclusion criteria

Exclusion criteria: Persons who meet the following conditions will be excluded from participation in this study -Those who have had more than 10 hours of OD training in the past. -Those who have obvious difficulties in following up during the study period. -Those who, in the opinion of the principal investigator, have a serious physical or mental illness that would make it difficult for them to participate in the study. -Those who the principal investigator determines are not appropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
The primary outcomes will be 1) study inclusion rate, 2) dropout rate, and 3) training participation rate. The study inclusion rate will be the number of participants/number of applicants, the dropout rate will be the number of dropouts/number of study subjects (study subjects who participated in training less than four times will be considered dropouts), and the training participation rate will be the number of times participated/8 times.

Secondary

MeasureTime frame
Secondary endpoints in this study were NAS (EE scale), FCJ (EE scale), SOC-13 (SOC scale), PSS (stress scale), DSS (stigma scale), SDS (social distance), PS (psychological safety scale), UWES (work engagement scale), SCS ( Self-Compassion Scale), and WHO-HPQ (Labor Productivity) at the beginning of the study (week 0), at the end of the intervention (week 8), and at follow-up (week 16), as well as the mean and standard deviation.

Countries

Japan

Contacts

Public ContactMasashi Yamada

Keio University School of Medicine Department of Neuropsychiatry

yamada.masashi@keio.jp+81-(0)3-3353-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026