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Pursuing the Triple Aim in Hotspotters: Identification and Integrated Care

L

Leiden University Medical Center (LUMC)

Status

Invitation-only

Conditions

Psychosocial Problem
Chronic Disease
Multimorbidity
Complex Patient

Treatments

Other: Proactive, integrated and personalised care

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Hotspotters are patients with complex care needs, defined by problems in multiple life domains and high acute care use. These patients often receive mismatched care, resulting in overuse of care and increased healthcare costs. Reliable data on (cost-)effective interventions for these patients are scarce. The goal of this study is to assess the cost-effectiveness of pro-active and integrated care. This approach includes: an intake consultation with Positive Health; multidisciplinary meetings with physician, mental healthcare nurse, social worker and the patient; a personalised care plan and proactive care management. We aim to include 200 patients, divided over 20 primary care practices.

Full description

People with complex problems on multiple life domains, so called 'hotspotters', receive fragmented care. This is difficult to manage by patients and care providers , leading to little effect of care and persistent unmet needs. The accumulation and complexity of problems often leads to high medical expenses. Next to their high medical spending levels, hotspotters´ experiences with the healthcare system are low as the healthcare system is not (yet) successful in dealing with their needs. Interventions aimed at the complex situation of hotspotters in our current healthcare system might benefit by applying a Triple Aim approach. This approach aims to simultaneously improve the individual experience of care, reduce the cost of care per capita and improve the health of populations by offering proactive integrated care.

Is proactive integrated care costeffective and does it result in better patients experience than usual care after 12 months for patients with problems on multiple life domains? The intervention consists of: intake consultation assessing health on multiple domains using positive health or similar tool; multidisciplinary meetings with physician, mental healthcare nurse, social worker and patient, personalised care plan and proactive care management.

This stepped wedge cluster RCT aims to include 200 patients, divided over 20 primary care practices. All practices start with an observation period (2-8months), followed by the intervention (12 months) and follow-up (2-8months). Total duration of intervention is 22 months. We define Hotspotters as patients with at least two incidents of acute care utilisation (defined as out-of-office GP consultations, acute psychiatric care, emergency department visits and unplanned admissions) during the past year, and problems on two out of three health domains (chronic somatic, mental and/or social problems) based on diagnosis (coded with the International Classification of Primary Care) or medication (ATC) coding.

Primary outcome: Incremental cost-effectiveness from a societal perspective. Information on cost will be based on patient-reported data obtained by questionnaires supplied with data from the GP medical files (Huisarts informatie system, HIS) and CBSmicrodata. To assess the effectiveness the EQ-5D-5L will be used for determining quality of life.

Secondary outcomes: Insight into patients experience of care, quality of life, proactive coping, and self-efficacy. This information will be gathered using interviews, focus groups and questionnaires (SF-12, UPCC, PAM-13 and SE+IN itemlist). Process evaluation with the involved care professionals, integration level, the nature of the communication between healthcare provider and patient (HCCQ, OPTION5), and acceptability (AIM), appropriateness (IAM), feasibility (FIM) ,and perceived and experienced effectiveness of the intervention.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patients are ≥ 18yrs
  • The patients are registered within one of the participating GP practices.
  • Patients with at least two acute care encounters in the past 12 months. Acute care encounter is defined as an encounter with out-of-hours GP service, emergency care or acute mental health care.Patients have problems registered in the GP Information system on at least two out of three of the following domains: somatic, mental or social. Somatic problems is having at least one ICPC code on the problem list. Mental problems is having at least one ICPC code from the "P"-chapter on either the problem list, as a reason for encounter, and/or having medication prescribed related to mental health problems. Social problems is having at least one ICPC code from the "Z"-chapter or as reason for encounter, and/or having medication prescribed related to social problems.

Exclusion criteria

  • The patient is terminal.
  • The patient is living in a residential home.
  • The patient has dementia or a disability that prevents them from communicating effectively.The patient already has experience with the positive health tool.
  • The patient is not competent to make decisions concerning their health. This wil be assessed by the patient's own general practitioner.
  • Veto of the GP

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

200 participants in 4 patient groups

Control period 2 months
Other group
Description:
2 months control period, followed by 12 months intervention, followed by 8 months observation
Treatment:
Other: Proactive, integrated and personalised care
Control period 4 months
Other group
Description:
4 months control period, followed by 12 months intervention, followed by 6 months observation
Treatment:
Other: Proactive, integrated and personalised care
Control period 6 months
Other group
Description:
6 months control period, followed by 12 months intervention, followed by 4 months observation
Treatment:
Other: Proactive, integrated and personalised care
Control period 8 months
Other group
Description:
8 months control period, followed by 12 months intervention, followed by 2 months observation
Treatment:
Other: Proactive, integrated and personalised care

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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