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Behavioral Intervention
Telehealth Cognitive Behavioral Therapy for Alcohol Abuse with Cardiovascular Risk (ACME-TM Trial)
N/A
Recruiting
Led By Daniel Blalock, PhD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosis of hypertension, hyperlipidemia, and/or diabetes mellitus in EHR (ICD-10 codes I10, E78.xx, and E11.xxxx) for at least one year.
Be older than 18 years old
Must not have
Current palliative care or care through a nursing/hospice home.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months post-baseline
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a cognitive-behavioral intervention for Veterans with comorbid alcohol misuse and cardiovascular disease risk. The intervention includes telehealth CBT for alcohol misuse, tailored and timely text messages, and a telehealth coaching call. The primary hypotheses are that the intervention will be feasible, acceptable, and show signs of reducing alcohol misuse and increasing behaviors associated with cardiovascular health.
Who is the study for?
This trial is for Veterans with uncontrolled high blood pressure, hyperlipidemia, or diabetes who misuse alcohol. They must be enrolled in specific VA clinics, have a history of these conditions for at least a year, take medication for them, and have access to text messaging. Excluded are those in other CVD or alcohol treatment trials, with severe alcohol dependence or significant withdrawal symptoms.
What is being tested?
The ACME-TM program combines cognitive-behavioral therapy via telehealth and mobile health technologies to reduce alcohol misuse and improve cardiovascular health behaviors among veterans. It includes personalized text messages and coaching calls focused on transitioning treatment targets.
What are the potential side effects?
Since this intervention involves behavioral therapy rather than medication, typical drug side effects aren't expected. However, participants may experience stress or discomfort discussing personal habits like drinking during the counseling sessions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with high blood pressure, high cholesterol, or diabetes for over a year.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently receiving palliative care or am in a nursing/hospice home.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months post-baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months post-baseline
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Enrollment Feasibility
SMS Text Acceptability
Therapist Fidelity
+2 moreSecondary study objectives
Past-Month Self-Reported Heavy Drinking Days
ReComp Pharmacy Refill Compliance Estimate for CVD medications
Systolic Blood Pressure
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: ACME-TMExperimental Treatment1 Intervention
Participants will obtain 4 sessions of telehealth cognitive behavioral therapy (CBT) focused on reducing alcohol misuse. Participants will receive a 5th telehealth coaching call to develop a plan for ensuing treatment regarding their elevated cardiovascular risk factors. Participants will then receive daily texts for one month aimed at helping them decrease these cardiovascular risk factors.
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Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,663 Previous Clinical Trials
3,427,248 Total Patients Enrolled
Daniel Blalock, PhDPrincipal InvestigatorDurham VA Medical Center, Durham, NC
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I don't have any upcoming surgeries or need major changes to my medications.My medication for heart disease prevention has been approved by the research team.I am currently receiving palliative care or am in a nursing/hospice home.My medication for preventing heart disease is not suitable for the trial.I have been diagnosed with high blood pressure, high cholesterol, or diabetes for over a year.I am taking medication for high blood pressure, high cholesterol, or diabetes.
Research Study Groups:
This trial has the following groups:- Group 1: ACME-TM
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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