Strasbourg, 3 July 2020                                                                                      DH-BIO/INF (2020) 5

Addendum

COMMITTEE ON BIOETHICS (DH-BIO)

ADDENDUM

to the Compendium of good practices in mental health care

- how to promote voluntary care and treatment practices -

Collection of examples

July 2020 – December 2020

Replies to be submitted using the form below by e-mail

to the Secretariat of the Committee on Bioethics

____________

Person responsible within the Secretariat:

Ms Katrin Uerpmann, tel. +33 (0) 390 21 43 25

a)   Essential information (necessary for inclusion in the compendium)

Name of the practice:       Address of the place where the practice is carried out:

1.   In which areas is the practice implemented (healthcare, employment, housing, training/education, social policies…)?

     

2.   If the practice is linked to healthcare, at which stage of the health care path is it implemented (general health care, admission, follow up…)?

     

3.   What is the aim of the practice?

     

4.   Does the practice address a specific situation (crisis situation, follow-up to hospitalisation, homelessness...)?

     

5.   Individuals concerned (persons with specific mental health needs, specific groups such as adolescents/young adults, elderly persons, health care professionals…)?

     

6.   Scope or area of the practice: national/regional/local?

     

7.   Detailed description of the practice and how it is carried out, including length and frequency, if applicable.

     

8.   Indicator of the impact of the practice(feedback from service users/family members/service providers/health professionals; decrease of recourse to involuntary measures…), including any available information on the medium- or long-term impact of the practice.

     

b) Additional useful information (to be submitted only if available)

9.   Factors which have facilitated the implementation of the practice.

     

10.         Information on the barriers to the implementation of the practice, if any.

     

11.         Which other options were available?

     

12.         Which factors are considered essential for transferability of the practice into a different setting?

     

13.         Formal assessment of the impact of the practice (external or self-evaluation)

     

14.         Cost evaluation (costs/saving analysis)

     

15.         How were the service users involved in the decision-making process leading to the implementation of the practice?

     

16.         Any additional feedback from stakeholders (service users, family members, health professionals, social workers etc.)

     

17.         Any additional statistical information relating to the short-, medium- or long-term impact of the practice

     

18.         Information on any on-line or other resources (tool kits, guides, reports…)

     

19.         Detail of a contact personwho could be contacted to request further information, if needed.