Your session is about to expire
← Back to Search
Social Network vs Individual Counseling for Post-Stroke High Blood Pressure (TEAMS-BP Trial)
N/A
Recruiting
Research Sponsored by Brigham and Women's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
21 years of age or older
Within 14 days after stroke
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
TEAMS-BP Trial Summary
This trial will compare whether a social network intervention or individual hypertension counseling is more effective in reducing blood pressure after stroke.
Who is the study for?
This trial is for adults over 21 who have high blood pressure and have experienced their first ischemic stroke recently. They must be able to consent, participate in interviews, and use text messages. It's not for those with severe speech difficulties, life expectancy under 6 months, dementia, a history of strokes or an NIHSS score over 21.Check my eligibility
What is being tested?
TEAMS-BP study compares social network group counseling against individual counseling to manage blood pressure after a stroke. Participants are split into groups based on their social network size and given different types of support to see which method better controls blood pressure.See study design
What are the potential side effects?
Since the interventions involve counseling rather than medication, typical drug side effects aren't expected. However, participants may experience stress or emotional discomfort discussing health issues within a group or individual setting.
TEAMS-BP Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 21 years old or older.
Select...
I had a stroke less than 14 days ago.
Select...
I have had my first stroke, confirmed by a doctor or imaging.
Select...
I had a stroke less than a week ago.
TEAMS-BP Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Systolic Blood Pressure
Secondary outcome measures
Achievement of post-stroke hypertension treatment goal
Patient reported physical function
TEAMS-BP Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Social Network CounselingExperimental Treatment1 Intervention
The index patient and influential social network members will meet via Zoom 3 times over the course of 3 months with a clinical research nurse for teamwork counseling and blood pressure education.
Group II: Individual CounselingActive Control1 Intervention
The index patient will meet via Zoom 3 times over the course of 3 months with a clinical research nurse for blood pressure education.
Find a Location
Who is running the clinical trial?
Brigham and Women's HospitalLead Sponsor
1,612 Previous Clinical Trials
11,470,515 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have significant difficulty with speaking or understanding language.I am 21 years old or older.I have chosen not to participate in research as noted in my medical records.You have a medical condition that is likely to cause death within 6 months.I am unable to give consent or participate in interviews.I have a history of high blood pressure or started blood pressure medication recently.I have been diagnosed with dementia.I have had my first stroke, confirmed by a doctor or imaging.I had a stroke less than 14 days ago.Your NIH Stroke Scale score is higher than 21.I have had a stroke before.I had a stroke less than a week ago.
Research Study Groups:
This trial has the following groups:- Group 1: Social Network Counseling
- Group 2: Individual Counseling
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the greatest number of subjects enrolled in this medical experiment?
"Affirmative. Reports on clinicaltrials.gov verify that this trial, which was initially launched at the end of May 2022 is actively recruiting for 60 patients from a single medical facility."
Answered by AI
Is the door open to individuals seeking this clinical trial?
"Clinicaltrials.gov shows that this specific study is actively recruiting patients, having been published on May 31st 2022 and updated most recently on June 30th 2022."
Answered by AI
Who else is applying?
What state do they live in?
Massachusetts
How old are they?
18 - 65
What site did they apply to?
Brigham and Women's Hospital
What portion of applicants met pre-screening criteria?
Did not meet criteria
Met criteria
Share this study with friends
Copy Link
Messenger