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The InterACT (Intervention for Appropriate Care and Treatment) study: working with clinical teams in hospitals to trial a feedback loop approach to promoting appropriate care and treatment for elderly patients at the end-of-life.

A stepped-wedge randomised-controlled trial assessing the implementation, impact and costs of a prospective feedback loop to promote appropriate care and treatment for elderly patients in acute hospitals at the end of life.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000675123
Acronym
InterACT: Intervention for Appropriate Care and Treatment
Enrollment
4677
Registered
2019-05-06
Start date
2020-02-10
Completion date
2021-08-20
Last updated
2024-04-22

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

Conditions

None listed

Brief summary

This study will work with clinical teams in three acute hospitals to trial a feedback loop approach to promoting appropriate care and treatment for elderly patients at the end-of-life. The feedback loop is intended to provide a ‘flag’ to increase clinician awareness of the risk profile of their patients, and to prompt a tailored care review activity. It is expected that the use of this feedback intervention will improve care outcomes for elderly patients, specifically to increase appropriate care and treatment pathways and reduce the incidence of non-beneficial treatments. the study will report the impact on patients, and the costs and implementation issues of the feedback loop activity.

Interventions

The study intervention involves a prospective feedback loop to clinical teams, based on the outcomes of a twice-weekly patient record review process using the Criteria for Screening and Triaging to Appropriate aLternative Care (CriSTAL) tool and the Supportive and Palliative Care Indicators Tool (SPICT). The feedback provided to the clinical teams (the CriSTAL status and SPICT score) is intended to act firstly as a flag for the clinical team to review patient care activities and pathways, and to

The study intervention involves a prospective feedback loop to clinical teams, based on the outcomes of a twice-weekly patient record review process using the Criteria for Screening and Triaging to Appropriate aLternative Care (CriSTAL) tool and the Supportive and Palliative Care Indicators Tool (SPICT). The feedback provided to the clinical teams (the CriSTAL status and SPICT score) is intended to act firstly as a flag for the clinical team to review patient care activities and pathways, and to stimulate a tailored clinical response to promote appropriate patient care and treatment outcomes. The study will be implemented in three acute Queensland hospitals. All hospitals commence the study at the same time point, and all complete a four-week site preparation and clinical team recruitment phase. Hospital 1 then sequentially completes a 16 week usual exposure phase, a four-week intervention establishment phase and a 34-week intervention exposure phase; Hospital 2, a 25-week usual exposure phase, a four-week establishment phase and a 25-week intervention exposure phase; and Hospital 3, a 34-week usual exposure phase, a four-week establishment phase and a 16-week intervention exposure phase. The four-week intervention establishment phase will be used to prepare for the implementation of the feedback loop intervention, and tailor it to ensure it is feasible at each site and reflects local context and workflows. In this phase the the project team, study team, hospital executive advisory group and enrolled clinical teams will work together to: - attend information sessions about the study, the tools being used, the background and evidence for non-beneficial treatment including risk factors and the range of options for responding to screened patients. these will be delivered by the project team. Number and duration will be tailored to reflect hospital requirements; will minimally include a 30 minute introduction session and a 30 minute evidence and rationale session. - decide the process for the study team to provide the patient level screening outcomes to the clinical teams: - pilot the proposed feedback mechanisms for one week with each clinical team, in the intervention establishment phase. - decide the preferred clinical team responses to feedback. This will require agreement on how each clinical team will respond to feedback about the screening outcomes and the hospital inputs that will be provided to support this. Clinician response plans could include, but will not be limited to, palliative care referral, multidisciplinary team review, advance care planning consultation, and patient/carer meetings. The record review will be performed by a trained auditor, employed as a Registered Nurse at the participating hospital and not part of the participating clinical team. A member of the study team will provide direct feedback to a nominated clinical team member of the outcomes of each record review. The study team will conduct a process evaluation to assess adherence and fidelity and support implementation. The record review will occur throughout the usual exposure, intervention establishment and intervention exposure phases, with the feedback of the screening scores to clinical teams and a tailored clinical response part of the intervention phase only. There are three participant populations across the study: 1: Clinical teams - who will be enrolled in the study and participate in the feedback loop intervention 2: Patients 75 years and older, admitted under enrolled clinical teams 3: Members of the enrolled clinical teams, executive advisory group, site study team - who will be invited to participate in semi-structured interviews in the intervention establishment, intervention exposure and post-trial phases.

Sponsors

Queensland University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Note that this study directly recruits clinical teams to participate not patients. Inclusion criteria for Population 1, Clinical teams: - be an established clinical team unit or specialty that routinely admits patients within the hospital - include a nominated lead specialist consultant/s - include a registrar/s and affiliated clinical nurse consultant or nurse unit manager - have a clinical team structure and admission pattern typical of the hospital - have a consistent history of admitting patients aged 75 years or over during a sample time period in the previous year - participate in an information session with the project team. Inclusion criteria for Population 2, patient data: Patients admitted under the enrolled clinical teams and aged 75 years or over. Inclusion criteria for population 3, (semi-structured interviews), Clinical teams, executive advisory group, site study team: Enrolled clinical teams, hospital study executive advisory group and site study team members.

Exclusion criteria

Clinical team exclusion criteria: Excluded clinical teams will be those from the emergency department, any Intensive Care Units (ICUs), mental health units, and non-acute care and teams that do not meet all the inclusion criteria. While inappropriate treatment can occur in the ICU setting, we are choosing to study the feedback intervention with clinical teams that care for patients before they go to ICU. Clinical teams that are already implementing an intervention or initiatives related to reducing non-beneficial treatments for older patients will be excluded. Exclusion criteria patient data: Patients <75 years of age or not admitted under the enrolled clinical teams. Exclusion criteria, semi-structured interviews: Clinical teams not enrolled in the intervention.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 17, 2026