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NCT Number: NCT06414317

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Roswell Park Cancer Institute

Buffalo, New York, 14263, United States

Location status: Recruiting

Location contact

Saby George, MD

CONTACT

[email protected]

716-845-3159

Saby George, MD

PRINCIPAL_INVESTIGATOR

About this study

PRIMARY OBJECTIVES:

I. To assess project readiness and barriers and requirements to assure success we will evaluate organizational readiness and implementation climate through stakeholder engagement.

II. Development of an ENST to meet the needs of patients and caregivers, the delivery of which is deemed feasible based on such pre-implementation assessment.

III. Implementation and delivery of the proposed ENST. IV. Facilitation of enhanced care coordination for patients with advanced bladder cancer who often have complex medical needs, using measures elaborated in the design and methods section.

V. Determining the impact of such interventions, in a quantifiable manner, using validated instruments to assess perceptions of care coordination and self-efficacy, as well as monitoring concordance with guideline-recommended care by leveraging data from a network-wide decision support tool that captures systemic therapy selections.

OUTLINE:

Patients and caregivers receive access to the bladder cancer ENST and patients undergo psychological distress and nutrition screenings and may attend social work, psychology, and/or nutrition consultations as appropriate throughout the study. Patients, caregivers, and providers also attend virtual support group meetings periodically on study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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
  • PATIENTS: Able to speak, understand, read, and write English
  • CAREGIVERS: Age ≥ 18 years
  • CAREGIVERS: Only caregivers of enrolled patients will be included in the study
  • CAREGIVERS: Should be able to speak, understand, read, and write English
  • CAREGIVERS: Caregivers will be enrolled in the study during the same time window as for patient enrollment (from initial visit to within 8 weeks of patients starting frontline therapy)

Exclusion criteria

  • 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
  • CAREGIVERS: Cognitively impaired adults/adults with impaired decision-making capacity
  • CAREGIVERS: Individuals who are not yet adults (infants, children, teenagers)

Treatment and study plan

Assessment of Distress

Procedure

Undergo psychological distress screening

Other names: Assessment of Psychological Distress, Evaluation of Patient's Distress

Consultation Visit

Other

Attend consultations

Nutritional Assessment

Other

Undergo malnutrition screening

Other names: Dietary Assessment, dietary counseling, nutritional counseling

Questionnaire Administration

Other

Ancillary studies

Supportive Care

Other

Receive access to bladder cancer ENST

Other names: Supportive Therapy, Symptom Management, Therapy, Supportive

Primary outcomes

  1. Organizational readiness for implementing change (ORIC)

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

    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)

  2. Guideline-concordant care at the institutional level

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

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

  3. Patient perception of care coordination

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

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

  4. Patient perception of self-efficacy

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

    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).

  5. Caregiver perception of care coordination

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

    Caregiver perception of care coordination will be measured using Care Coordination Instrument for Caregivers.

Sponsors and collaborators

Lead sponsor

Roswell Park Cancer Institute

Other

Registry information

Official study title

A Comprehensive Education and Navigational Support Program for Advanced Bladder Cancer

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
May 16, 2024
Registry last updated
Jan 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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