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Telehealth Group Counseling and Preventive Care for Women

Utilizing Telehealth Group Counseling Sessions to Improve the Process and Delivery of Secondary Preventive Care for Women With Atherosclerotic Cardiovascular Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06404515
Enrollment
13
Registered
2024-05-08
Start date
2024-07-10
Completion date
2024-11-14
Last updated
2025-06-24

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

Conditions

Acute Coronary Syndrome, ASCVD, Chest Pain, Coronary Artery Disease, Myocardial Infarction, NSTEMI, STEMI, Unstable Angina

Keywords

ASCVD, NSTEMI, STEMI, Coronary Artery Disease, ACS, Myocardial Infarction, Unstable Angina, Chest Pain

Brief summary

The purpose of this study is to utilize an innovative healthcare delivery strategy via telehealth group counseling sessions to improve engagement, adherence, and ultimately outcomes in female patients with atherosclerotic cardiovascular disease (ASCVD).

Detailed description

This will be an electronic survey study of female patients with known atherosclerotic cardiovascular disease (ASCVD) who are managed by providers in the Weill Cornell Medicine Cardiology Division and self-select into this telehealth group education series. Group health counseling will be administered via the Weill Cornell Medicine approved telehealth platform at the time of participation. Participants will have the option to choose the session topic of their choice and will have the opportunity to participate in 1-5 sessions over 12 weeks, depending on their preference. Each session will occur regardless of number of participants but will be capped at 12 participants, anticipating that two will not join. Once consent is obtained, baseline characteristics of participants will be collected via chart review. Demographics such as age, race, insurance carrier, and clinician-documented diagnoses, such as ASCVD, hypertension (HTN), hyperlipidemia (HLD), and diabetes mellitus (DM), will be collected. Prior to each group health counseling session, an initial survey will be provided to patients who are chosen for and consent to this study. This survey will ask patients about their demographics, self-reported diagnoses, current level of satisfaction about their understanding of their diagnoses, reasons for participating in the study, and history of previous participation in telehealth group counseling. After the sessions, a post-session survey will be provided to all participants and will assess patient understanding, including diagnoses and medications, satisfaction with the format, satisfaction with the provider, how many sessions were attended, reasons for attending more than one session, and recommendation of this format to others. All data will be de-identified prior to analysis and will remain confidential among investigators.

Interventions

OTHERTelehealth Group Counseling

Group counseling for women via telehealth to provide educational materials about atherosclerotic heart disease and provide information about risk factors and modification of risk factors. Women then have an opportunity to discuss / ask questions.

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Subjects will participate in at least one telehealth session, lasting one hour, or up to five sessions lasting one hour each, over the course of 12 weeks.

Eligibility

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

Inclusion criteria

* Female patients * Age 18 and older * Patients who are managed by providers at the Weill Cornell Medicine Women's Heart Program * Women with evidence of atherosclerotic cardiovascular disease (ASCVD) and diagnoses of chest pain, myocardial infarction/heart attack (myocardial infarction - non ST elevation NSTEMI, ST elevation STEMI), coronary artery disease, acute coronary syndrome, unstable angina, atherosclerotic cardiovascular disease, hypertension (HTN), hyperlipidemia (HLD), diabetes (DM), and/or palpitations (as confirmed by clinician referral to study and chart review)

Exclusion criteria

• Women with risk factors (ex: HTN, HLD, DM) but no evidence of ASCVD

Design outcomes

Primary

MeasureTime frameDescription
Change in patient's accessibility to care as assessed by Likert scale.Immediately Before and Immediately After Each Counseling Session, up to 12 weeksScore ranges from 0 to 5 with 0 being not satisfied and 5 being very satisfied.
Change in patient's understanding of their disease as assessed by Likert scale.Immediately Before and Immediately After Each Counseling Session, up to 12 weeksScore ranges from 0 to 5 with 0 being not satisfied and 5 being very satisfied.
Change in medication compliance as assessed by Likert scale.Immediately Before and Immediately After Each Counseling Session, up to 12 weeksScore ranges from 0 to 5 with 0 being not likely and 5 being very likely.
Change in overall patient satisfaction as assessed by Likert scale.Immediately Before and Immediately After Each Counseling Session, up to 12 weeksScore ranges from 0 to 5 with 0 being not satisfied and 5 being very satisfied.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026