Goal-setting in Stroke: From Guideline Towards Implementation: a Realist Evaluation

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Overall objective: The aim of the project is to integrate the quality improvement programme on goal setting into the current care of people with stroke and to test and refine this programme. Target group: 1. People after a stroke (treatment in the participating centres); total number 155 people 2. Informal carers (only if the person has had a stroke and has limited opportunities to participate) 3. Professional carer; total number 155 people What? The goal-setting programme becomes standard care, it is checked whether the programme has been applied in care by health professionals (review of the patient's medical record), what the effects are on patients (questionnaires) and health professionals (questionnaires) and whether the quality improvement programme needs to be adjusted or refined (interviews with health professionals and the patient group) When to evaluate? 1. Health professionals: start of the study and end of the study via questionnaires. Interviews/focus group (every 3 months) 2. Review of patient records and observations (every 3 weeks) 3. Patient assessment: Admission and 1 week before discharge or end of study, Interviews/focus group (3 months)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Participants are employed in hospitals, rehabilitation centres and/or private practices/primary healthcare facilities located in the provinces: Province of Flemish Brabant, Brussels, Province of Walloon Brabant, Limburg

• Participants have a social, medical profession/background, work in the management of healthcare services or quality of healthcare

• Participants involved (direct or indirect) in the goal-setting process of the patients

• Participants who master the Flemish or French language

• Adult participants (≥18 years)

• Participants after a stroke event.

• Residence in one of the four participating sites, in outpatient care or receive treatment in first line zone

• Participants who master the Flemish or French language

• Adult participants (≥18 years)

⁃ • Informal caregiver of a stroke patient admitted to one of the four participating sites

Locations
Other Locations
Belgium
UHasselt
RECRUITING
Hasselt
Contact Information
Primary
Annemie Spooren, prof dr
annemie.spooren@uhasselt.be
+3211269332
Time Frame
Start Date: 2023-01-17
Estimated Completion Date: 2024-03-30
Participants
Target number of participants: 280
Treatments
Experimental: People after a stroke event
Implementation of improvement program
Experimental: Healthcare professionals
Implementation of improvement program
Experimental: Close relatives of people after a stroke
Implementation of improvement program
Related Therapeutic Areas
Sponsors
Leads: Hasselt University
Collaborators: Federal Public Service Health, Food Chain Safety and Environment

This content was sourced from clinicaltrials.gov