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Implementing Shared Decision Making in Interprofessional Home Care Teams

Implementing Shared Decision Making in Interprofessional Home Care Teams : a Stepped Wedge Cluster Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02592525
Acronym
IPSDM-SW
Enrollment
653
Registered
2015-10-30
Start date
2015-11-30
Completion date
2018-12-31
Last updated
2019-12-20

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

Conditions

Aging

Brief summary

This study will train health providers in home care teams across Quebec in shared decision making about the decision to stay at home or move to another location. This decision is one of the toughest for older Canadians. Decisions that are informed, shared and supported produce better results. An interprofessional approach to shared decision making is when older persons and their caregivers are supported by not just one but by all the professionals involved in their care.The impact of the training program in interprofessional shared decision making (IPSDM) above that of the passive dissemination of a decision guide will be assessed by measuring to what extent older persons caregivers say they took active part in the decision-making process. Other outcome measures will be: i) what option they chose, whether they feel conflict or regret about their decision, and the burden of care they feel; ii) the quality of life of clients;

Interventions

BEHAVIORALIP-SDM training for health professionals

Multifaceted SDM training program for providers: i) 1.5-hour online tutorial, ii) 3.5-hour skills building workshop; iii) video-clip demonstrating SDM in the context of an IP home care team with an aging adult making a decision about location of care (to be used with clients and providers as well); and iv) performance feedback to providers (role play during the workshop).

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
CHU de Quebec-Universite Laval
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

Clients or caregivers of clients : * Aged ≥65 years; * Receiving care from the IP home care team of the enrolled CISSS/CIUSSS * Have made a decision about whether to stay at home or move to another location during the recruitment periods * Are able to read, understand and write French or English * Can give informed consent In the case clients are not able to provide informed consent, their caregiver will be eligible.

Exclusion criteria

* Clients who are not able to provide informed consent and who don't have a caregiver

Design outcomes

Primary

MeasureTime frameDescription
Assumed Role in decision making7 monthsTo assess the proportion of caregivers reporting an active role, a modified version of the Control Preferences Scale designed to assess the role assumed in the decision making process will be used. The scale consists of a single question and is the one most frequently used in studies assessing the implementation of SDM in clinical practice.

Secondary

MeasureTime frameDescription
Decisional Regret7 monthsAssessed with the Decisional Regret Scale
Decisional Conflict7 monthsAssessed with the Decisional Conflict Scale
Patient involvement in decision making7 monthsAssessed with the Dyadic-OPTION scale, a 12-item self-administered instrument that assesses 12 specific SDM behaviours during the decision-making process
Burden of care7 monthsAssessed with the Zarit Burden Inventory Scale (ZBI), caregivers only
Preferred and chosen option (remain at home or move to another location)7 monthsQuestionnaire assessing the prefered and chosen option
Health-related quality of life7 monthsAssessed with two subscales (Social isolation and Emotional reactions) of the HR-QoL questionnaire from the Nottingham Health Profile, clients only

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026