Service users were not routinely involved in the organization of their care |
A patient‐held record is now being developed to support patients in making their own records about care they receive |
Patients were not routinely asked to become involved in the design of their care plans, or to sign them |
Patient signatures now required on care plans, and a record made of their involvement/understanding |
Changes to organization of therapeutic activity require information from service users |
Questionnaire sent to recently discharged service users asking for their views regarding the activities that would be most helpful to them. Responses aid the reorganization process |
Patients requested more regular discussion regarding ward issues, with the nursing team |
Regular community meetings are now held on the ward. All patients invited to attend. Patients decide agenda for each meeting |
Difficulty assessing patient's experiences relating to the collaborative improvement measures |
All patients now invited to complete questionnaire relating to MHC improvement measures. Opportunity made for postal returns. Responses demonstrated service user satisfaction with the changes |
Difficulty effectively communicating with patients regarding the aims of the project, changes made and current plans |
MHC newsletter now given to all patients to explain project, detail changes made and provide overview of planned changes |