- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT06904144
Gezondheidscoaching voor patiënten met hart- en vaatziekten
Gezondheidscoaching voor patiënten met hart- en vaatziekten: een evaluatie van gemengde methoden van de impact op de resultaten van de patiënt en de tevredenheid en de aanvaardbaarheid van de provider
For patients discharged with a diagnosis of cardiovascular disease coronary artery disease resulting in myocardial infarction and/or congestive heart failure, this study will evaluate if the addition of 12 virtual health coaching sessions over the course of 16 weeks will improve physiological, psychological, and social health outcomes, prove acceptable and satisfactory for these patients with CVD, decrease CVD-related questions and concerns sent to the provider via MyChart, and reduce hospital readmission rates over a 90-day period as compared to patients discharged with the same diagnosis who receive standard post-discharge care. The study will also evaluate the perceptions of physician and advanced practice providers related to the health coach as part of the interprofessional team and the amount of time spent addressing CVD-related patient questions and concerns via MyChart messages.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
The purpose of this mixed methods study is to evaluate the impact of 12 virtual health coaching sessions, provided post-discharge, over the course of 16 weeks on: 1) patient physiological measure of weight; 2) patient-reported perceived stress, anxiety, depression, and medication adherence, and physical, emotional, and social lifestyle behaviors; and 3) MyChart messaging to their providers related to concerns and/or questions about their cardiovascular diagnosis. The study will also assess: 4) patient acceptability and satisfaction with the health coaching intervention; 5) acceptability and satisfaction value and/or importance of the health coach intervention and feasibility of integrating the health coach into the inter-professional care team from the provider perspective; impact of the health coaching intervention on provider time spent on addressing MyChart messages; and 6) 30-, 60-, and 90-day hospital readmission rates.
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Beth Steinberg, PhD, RN
- Telefoonnummer: 614-406-7067
- E-mail: steinberg.35@osu.edu
Studie Contact Back-up
- Naam: Maryanna Klatt, PhD
- Telefoonnummer: 614-293-3644
- E-mail: klatt.8@osu.edu
Studie Locaties
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Ohio
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Columbus, Ohio, Verenigde Staten, 43210
- The Ohio State University Wexner Medical Center
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Contact:
- Beth Steinberg, PhD, RN
- Telefoonnummer: 614-406-7067
- E-mail: steinberg.35@osu.edu
-
Contact:
- Maryanna Klatt, PhD
- Telefoonnummer: 614-293-3644
- E-mail: Klatt.8@osu.edu
-
Hoofdonderzoeker:
- Beth Steinberg, PhD, RN
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-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- 18 years of age or older
- diagnosis of coronary artery disease resulting in myocardial infarction and/or congestive heart failure
- physical condition effectively managed by routine healthcare and not requiring urgent medical attention
- ability to communicate in English
- access to a working phone or computer and ability to communicate via phone or computer.
Exclusion Criteria:
- Patients who have had chest coronary artery bypass surgery
- Documented cognitive and/or major psychiatric disorders, including dementia, Alzheimer's, depression or anxiety uncontrolled by anxiolytic, anti-psychotic, and/or anti-depressants and/or PHQ-9 score 15-27 and GAD-7 score >15
- current alcohol or drug dependency
- resident of extended care/skilled facility
- prisoners or ward of state.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ondersteunende zorg
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Health Coaching Intervention Group
Participants will receive 12 health coaching sessions post-discharge over a 16 week period |
12 virtual health coaching sessions will be provided over a 16 week period by a certified health coach. |
|
Geen tussenkomst: Standard Care Group
Participants will receive usual post-discharge care over the 16 week period |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Body weight
Tijdsspanne: Baseline (day of hospital discharge) and at provider appointment in the ambulatory setting, 16 weeks post-hospital discharge
|
Patient body weight in kilograms will be obtained by clinical staff on hospital approved and calibrated electronic standing scales. The patient's body weight will be collected from the patient's electronic medical record. |
Baseline (day of hospital discharge) and at provider appointment in the ambulatory setting, 16 weeks post-hospital discharge
|
|
Hospital readmissions
Tijdsspanne: Hospital readmissions during the 30-, 60-, and 90-days post-hospital discharge for cardiovascular disease, documented in the electronic medical record
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Hospital readmissions for an inpatient stay, documented in the electronic medical record, after the hospital post-discharge for cardiovascular disease |
Hospital readmissions during the 30-, 60-, and 90-days post-hospital discharge for cardiovascular disease, documented in the electronic medical record
|
|
MyChart messages
Tijdsspanne: Over the course of 16 weeks, from hospital discharge to 16 weeks post-hospital discharge
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MyChart messages are questions or requests directed to the patient's provider that are related to the patient's cardiovascular disease diagnosis and hospitalization. These MyChart messages are entered into the electronic medical record by the patient and are directed to their provider, requiring an electronic or telephone response to the patient with a documented note entered by the provider relative to the follow-up provided to the patient. This outcome measure will be the number of MyChart messages entered by the patient and responded to by the provider. |
Over the course of 16 weeks, from hospital discharge to 16 weeks post-hospital discharge
|
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Perceived Stress
Tijdsspanne: Baseline (hospital discharge), 8 weeks post-hospital discharge, and 16 weeks post-hospital discharge
|
Perceived Stress Scale-10 (PSS-10). A 10-item self-report measure of perceived stress. It is a measure of the degree to which situations in one's life are appraised as stressful over the past month. The 4-point Likert Scale includes responses of 0 (never), 1 (almost never), 2 (sometimes), 3 (fairly often), and 4 (very often). Individual scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress. |
Baseline (hospital discharge), 8 weeks post-hospital discharge, and 16 weeks post-hospital discharge
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Medication Adherence
Tijdsspanne: Baseline, and at 8 weeks post-hospital discharge and at 16 weeks post-hospital discharge
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The Hill-Bone Medication Adherence Scale (MB-MAS) is a 9-item self-assessment of medication adherence relative to a variety of chronic diseases and conditions. Likert Scale responses to each of the nine statements include 1 (all of the time), 2 (most of the time), 3 (some of the time), and 4 (none of the time). Total scores range from 4 to 36 with higher scores indicating higher medication adherence. |
Baseline, and at 8 weeks post-hospital discharge and at 16 weeks post-hospital discharge
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Lifestyle Medicine Behavior Assessment
Tijdsspanne: Completed at baseline, at 8 weeks post-hospital discharge and at 16 weeks post-hospital discharge
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The Lifestyle Medicine Short Form is a 14-item self-assessment scale evaluating physical, emotional, social lifestyle behaviors. The assessment questions comprise core metrics that capture readiness to change, as well as health behaviors that are aligned with the six pillars of lifestyle medicine--physical activity, nutrition, sleep health, stress reduction, social connections, and risky substances. Questions have multiple responses based on information relating to the six pillars of lifestyle medicine. The first two questions related to Readiness to Change use a Likert Scale ranging from 0 (Not Ready) to 10 (Very Ready). Questions related to Motivation and Diet request that the participant denote different aspects of their diet. Physical exercise questions request specific days/times in minutes completed. Questions related to sleep request average hours of sleep per 24 hour period. Mood, connectedness with others, and substance use request types/amounts per week. |
Completed at baseline, at 8 weeks post-hospital discharge and at 16 weeks post-hospital discharge
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Acceptability of Intervention Measure
Tijdsspanne: Completed after the 16 week health coaching intervention for participants in the intervention group.
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The Acceptability of Intervention Measure (AIM) is a 4-item self-report assessment to evaluate the acceptability of the health coaching intervention. Each statement is scored with a 5-point Likert Scale that includes 1 (completely disagree), 2 (disagree), 3 (neither agree nor disagree), 4 (agree), and 5 (completely agree). Total scores ranges from 4-20 with higher total scores indicating higher acceptability. |
Completed after the 16 week health coaching intervention for participants in the intervention group.
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Patient Qualitative Comments
Tijdsspanne: Immediately after completion of the 16 week health coaching intervention; i.e. 16 weeks post-hospital discharge
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Patient perceptions of the health coaching intervention will be solicited with the following question prompts: 1) Can you provide feedback about your health coaching experience?; 2) Did working with the health coach help you meet your health goals?; 3) Would you recommend working with a health coach to others? |
Immediately after completion of the 16 week health coaching intervention; i.e. 16 weeks post-hospital discharge
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Provider Qualitative Comments
Tijdsspanne: Will be completed within one month of their patient completing the health coach intervention.
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Provider perceptions of the value of the health coach as part of the interprofessional team and the feasibility of integrating the health coach into the patient's care will be solicited via question prompts that will include: 1) Can you discuss your perceptions about the value of the health coach as a member of the patient's care team; 2) Were you able to review the health coaches notes in the patient's medical record? (if yes) Were the notes helpful to you during the patient's follow-up appointment(s), i.e. in addressing the patient's condition, their post-discharge recovery, adherence to medical instructions, progress or lack of progress?; 3) Can you provide your perceptions of the feasibility of integrating the health coach as part of the patient's care team? |
Will be completed within one month of their patient completing the health coach intervention.
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Patient Health Questionnaire (PHQ-9)
Tijdsspanne: Baseline, 4-, 8-, and 16 weeks post-discharge for all participants
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A 9-item depression module the Patient Health Questionnaire that scores each of the 9 DSM-IV criteria as "0" (not at all) to "3" (nearly every day); scores range from 9-27. |
Baseline, 4-, 8-, and 16 weeks post-discharge for all participants
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Generalized Anxiety Disorder-7 (GAD-7)
Tijdsspanne: Baseline, 4-, 8-, and 16 weeks post-discharge for all participants
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A 7-item screening tool assessing anxiety over the past 2 weeks. Questions are scored from "0" (not at all) to "3" (nearly every day). Scores range from 0-21. |
Baseline, 4-, 8-, and 16 weeks post-discharge for all participants
|
Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: Beth Steinberg, PhD, RN, Ohio State University
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 2024H0179
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
IPD that will be shared will include de-identified descriptive data for both the intervention and control groups, including gender, race, educational level and mean age. Additionally, cardiovascular disease diagnoses, hospital readmissions at 30-, 60-, and 90- days post-hospital discharge, and number of MyChart messages sent by the patient to their provider. Acceptability of the intervention descriptive data for the intervention group will also be included. Differences in mean scores between the intervention and control groups for weight (significance and effect sizes), perceived stress and medication adherence will be shared. De-identified, curated qualitative data that will be shared includes interview transcripts from both patients and providers, as well as the qualitative codebooks and thematic analysis.
IPD-tijdsbestek voor delen
12-30-2026 to indefinitely
IPD-toegangscriteria voor delen
De-identified and curated demographic, statistical data, study overview, study consent will be accessible to academic researchers and educators through a data accessibility link once the Qualitative Data Repository submission is finalized.
IPD delen Ondersteunend informatietype
- ICF
- ANALYTIC_CODE
- MVO
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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