An Education and Navigation Support Tool to Improve Participation in Care Coordination Among Patients With Locally Advanced, Metastatic and Unresectable Bladder Cancer and Their Caregivers

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRoswell Park Cancer Institute

About this trial

This clinical trial evaluates the impact of an education and navigation support tool (ENST) on patient and caregiver participation in care coordination for bladder cancer that has spread to nearby tissue or lymph nodes (locally advanced), to other places in the body (metastatic) or that cannot be removed by surgery (unresectable). Patients with advanced bladder cancer tend to be older, have multiple medical conditions and often have poor access to health care. An ENST may be an effective method to improve participation in treatment decision-making and care planning among patients with locally advanced, metastatic and unresectable bladder cancer and their caregivers.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

PATIENTS: Age ≥ 18 years

PATIENTS: Metastatic or locally advanced, unresectable bladder cancer

PATIENTS: Receiving or planning to receive systemic therapy for bladder cancer at Roswell Park Comprehensive Cancer Center (RPCCC)

PATIENTS: Subjects can be enrolled any time from initial diagnosis of advanced disease to within 8 weeks after initiation of first-line systemic therapy for advanced bladder cancer

Disqualifiers

PATIENTS: Not receiving any form of systemic therapy for bladder cancer due to Eastern Cooperative Oncology Group (ECOG) performance status (PS) > 3, co-morbidities, or inadequate organ function

PATIENTS: Predominantly small cell histology

PATIENTS: Adults with impaired decision-making capacity, assessed by the study team to be unable to participate in ENST-based education and surveys

PATIENTS: Pregnant women

Trial design

Design model

Single group

Treatments tested in this trial

  • Assessment of Distress

    Procedure/Surgery

    Undergo psychological distress screening

  • Consultation Visit

    Other intervention

    Attend consultations

  • Nutritional Assessment

    Other intervention

    Undergo malnutrition screening

  • Questionnaire Administration

    Other intervention

    Ancillary studies

  • Supportive Care

    Other intervention

    Receive access to bladder cancer ENST

  • Supportive Care

    Other intervention

    Attend virtual support group meetings

Treatment groups

160 Participants
are divided into 1 treatment group
Group A: Supportive Care (ENST)Experimental treatment 5 interventions

Trial outcomes

Primary outcomes

1

Organizational readiness for implementing change (ORIC)

A 12 item instrument used to determine how well employees feel they can implement the change in process .. Each item includes a scale from 1 (Disagree ) to 5 (Agree)

Time frame
At baseline and at 6 months post-implementation
2

Guideline-concordant care at the institutional level

Guideline-concordant care at the institutional level will be calculated as the percentage of all systemic treatment decisions captured in the Clinical Oncology Pathway.

Time frame
At baseline and at 6 months intervals for the study duration
3

Patient perception of care coordination

Patient perception of care coordination will be measured using Care Coordination Instrument.

Time frame
At baseline and at 3 and 6 months post-implementation
4

Patient perception of self-efficacy

Patient perception of self-efficacy will be measured using Generalized Self-Efficacy scale. A 10 item psychometric scale with 4 choice responses ranging from 1 (not at all true) to 4 (Exactly true).

Time frame
At baseline and at 3 and 6 months post-implementation

Secondary outcomes

Other outcomes

Sponsors and contacts

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