Kidney Diseases Clinical Trial
— ImPart-MultiOfficial title:
A Feasibility Trial of a Stakeholder-Enhanced, Lay-Navigator-Delivered Intervention to Improve the Decisional Partnership of Chronic Kidney Disease Dyads
We seek to explore the feasibility and acceptability of participation in a decision-support training program led by lay navigators. ImPart-Multi, an education-telehealth-based, is designed to empower Black chronic kidney disease patients (CKD) patients and their care partner to seek the resources and support needed to be activated allies when making health-related decisions. Participants, based on random assignment, will participate in survey completion at study start and at 12 and 24 weeks of enrollment, and will complete 1, 3, or 4 education sessions via telehealth or audio connection. Participants will also complete an interview to share their thoughts on the program and other factors of interest.
Status | Recruiting |
Enrollment | 64 |
Est. completion date | November 15, 2024 |
Est. primary completion date | October 15, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients 1. Electronic medical record (EMR) documented diagnosis of stage 3 or 4 CKD (2 estimated glomerular filtration rate [eGFR] between 45-15 within 90 days); and concurrent cardiometabolic disease (hypertension and/or diabetes) 2. Ability to speak and read English and complete baseline questionnaires; 3. Patients must have a care partner enrolled in the study - the team will assist any patient in identifying a care partner, if interested. Inclusion Criteria: - Care partner 1. Age =18; 2) Self-endorsing or identified by the patient as "a relative, friend, or partner that has a close relationship with you and who assists you with your medical decisions and who may or may not live in the same residence as you and who is not paid for their help"; 2. Ability to speak and read English and complete baseline questionnaires; 3. Care partners must have an enrolled patient. Exclusion Criteria: - Patients 1. Receiving hospice; 2. Receiving dialysis; 3. Medical record documentation of active unmedicated severe mental illness, moderate-severe dementia, suicidal ideation, uncorrected hearing loss, and active substance abuse. Exclusion Criteria: - Care partner 1. Self-reported unmedicated mental illness, mild-severe dementia, active suicidal ideation, uncorrected hearing loss, or active substance abuse ascertained by study introduction questioning. |
Country | Name | City | State |
---|---|---|---|
United States | University of Alabama at Birmingham | Birmingham | Alabama |
Lead Sponsor | Collaborator |
---|---|
University of Alabama at Birmingham |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Acceptability of Intervention and Study Procedures | Through qualitative interviews, participant reported experiences with the ImPart Multi intervention and trial procedures. | Baseline to 12 weeks Groups 1, 2 and 3; 24 weeks Group 4 | |
Primary | Feasibility of Intervention Delivery and Data Collection | Proportion of participants who complete assigned intervention group and study related assessments. | Groups 1, 2, 3 and 4 baseline through to 12 weeks; Group 4 only baseline to 24 weeks | |
Secondary | Decision-making process using the Decision Conflict Scale (DCS) | 16 items total; measures perceptions of uncertainty in choosing options, factors contributing to uncertainty and feeling that decisions were informed and values-based | baseline, and 24 weeks after baseline | |
Secondary | Decision-making process using the Social Support Effectiveness-Questionnaire | 25 items measuring perceptions of help received in last 3 months | baseline and 12 weeks after baseline | |
Secondary | Patient Wellbeing using the Kidney Disease Quality of Life Scale (KDQOL-36) | 36 items measure 3 components:physical health, mental health, and kidney disease health. | baseline and 12 weeks after baseline | |
Secondary | Care partner well being using the PROMIS Global Health 10 | 10 items measure global health-related quality of life in 2 domains, physical and mental health | baseline and 12 weeks after baseline | |
Secondary | Dyadic Interaction using the Dyadic Coping Inventory | 37 item instrument designed to measure perceived communication and dyadic coping in close relationships when one or both partners is stressed. | baseline and 12 weeks after baseline |
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