Heart Coherence Training on Vascular Ehlers-Danlos Syndrome Patients
NCT05994664 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2024-07-01
Summary
Vascular Ehlers-Danlos Syndrome (VEDS) is caused by pathogenic variants of the COL3A1 gene, resulting abnormal Type III collagen protein. This impacts the body's connective tissue and makes people with VEDS at high risk of spontaneous aortic and arterial rupture, pneumothorax, and hollow organ perforation across the age spectrum. Given this risk and high potential for lethality, VEDS is considered the most severe type of Ehlers-Danlos Syndrome. In addition, many patients experience chronic pain and fatigue, sleep disturbances, and mental health challenges. As is the case for many patients with chronic illness, stress, anxiety, and depression are often present over the course of the disease. Despite the antecedent, stress and anxiety trigger a sympathetic nervous system (SNS) response in the body, which, over a period of time, can have detrimental effects both physiologically and psychologically for patients. Recent studies have begun to use biofeedback techniques to teach patients non-pharmacological strategies for managing their autonomic nervous system. One such program, Heartmath®, has been successful in helping patients lower stress, anxiety, and systolic blood pressure. This pilot trial was established to assess the effectiveness of a virtually based heart coherence program in a population with a chronic aortopathy in an effort to establish a larger, multi-provider program that also encompasses other cardiovascular populations.
Conditions
- Vascular Ehlers-Danlos Syndrome
Interventions
- OTHER
-
Heartmath Intervention
The participants will all complete baseline surveys and paperwork including signed consent, psychometric surveys, demographic survey, and a brief, open-ended questionnaire about their feelings about living with VEDS. During the initial visit for the intervention group the same assessment will be included, however, they will also receive 10-15 of instruction on a basic Heartmath technique. Group participants will be asked to complete 5-10 minutes of HeartMath techniques 2x daily. Participants from both groups will have weekly virtual sessions that include the 3-step Protocol HRV assessment. However, each week the intervention group will receive an addition 10-15 minutes of training and advancement on HeartMath techniques as well as continued written and video reinforcement.
- OTHER
-
Control Group
The participants will all complete baseline surveys and paperwork including signed consent, psychometric surveys, demographic survey, and a brief, open-ended questionnaire about their feelings about living with VEDS. The initial visit will include an HRV assessment using the HeartMath sensor via the 3-step Protocol developed by the HeartMath Institute. Participants from both groups will have weekly virtual sessions that include the 3-step Protocol HRV assessment. After the CG has completed 8 weeks, they will then have access to materials related to the techniques that were taught to the HMI group to allow for therapeutic equality.
Sponsors & Collaborators
-
Southern Star Research
collaborator INDUSTRY -
Baylor College of Medicine
lead OTHER
Principal Investigators
-
Shaine A Morris, MD, MPH · Baylor College of Medicine
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Years
- Max Age
- 45 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-04-01
- Primary Completion
- 2026-06-01
- Completion
- 2028-01-01
Countries
- United States
Study Locations
More Related Trials
-
Safety and Efficacy of Endovascular Repair of Complex Aortic Pathology With Physician-modified Endovascular Grafts (PMEGs)
NCT04746677 ·Status: RECRUITING ·Phase: NA
-
Stimulating Amyloid Clearance in Cerebral Amyloid Angiopathy
NCT06421532 ·Status: ENROLLING_BY_INVITATION ·Phase: PHASE2
-
Physician-modified Endovascular Graft for Repair of Complex Thoracoabdominal and Abdominal Aortic Aneurysms
NCT04526938 ·Status: SUSPENDED ·Phase: NA
-
Assessment of the GORE® EXCLUDER® Conformable AAA Endoprosthesis in the Treatment of Abdominal Aortic Aneurysms
NCT02489539 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
A Phase I Evaluation of the Safety of the TriVascular Stent-Graft System in the Treatment of Abdominal Aortic Aneurysms
NCT00646048 ·Status: COMPLETED ·Phase: PHASE1
-
A Study in Patients with a Descending TAA or PAU Treated with the E-nya Thoracic Stent Graft System
NCT04381507 ·Status: TERMINATED
-
Assessment of the GORE® EXCLUDER® Conformable AAA Endoprosthesis In the Treatment of Abdominal Aortic Aneurysms
NCT03743142 ·Status: ACTIVE_NOT_RECRUITING
-
Investigation of the Neurovegetative Pattern in Patients With Thoracic Aortic Aneurysms (TAA)
NCT05703893 ·Status: ACTIVE_NOT_RECRUITING
-
Reduction of Myocardial Infarction by Preconditioning in Patients With Ruptured Abdominal Aortic Aneurysm
NCT00883363 ·Status: COMPLETED ·Phase: NA
-
Prediction of Abdominal Aortic Aneurysm Shrinkage After Stent-placement With Artificial Intelligence
NCT06250998 ·Status: RECRUITING
-
Clinical Outcomes and Radiation Safety After Endovascular Repair of Complex AAAs Using Fenestrated- Branched Devices
NCT02266719 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Clinical Study to Assess Safety and Effectiveness of the Zenith® Dissection Endovascular System in Patients With Aortic Dissection
NCT00526487 ·Status: COMPLETED ·Phase: NA
-
The NEXUS™ Compassionate Use Data Collection Study
NCT03420066 ·Status: COMPLETED
-
Cerebral and Spinal Protection of Xenon Post-conditioning in Patients Undergoing Aortic Dissection Repair
NCT02774096 ·Status: UNKNOWN ·Phase: NA
-
Limb Remote Ischemic Preconditioning Reduces Heart and Lung Injury After Abdominal Aortic Aneurysm Repair
NCT01344239 ·Status: COMPLETED ·Phase: NA
-
Adjunctive Treatment With Doxycycline to Enhance the Durability of Endovascular Aortic Aneurysm Repair
NCT00126204 ·Status: COMPLETED ·Phase: NA
-
Impact of Elastin Mediated Vascular Stiffness on End Organs
NCT02840448 ·Status: COMPLETED
-
Coronary Artery and Coronary Artery Bypass Graft Imaging Using a Specialized Catheter and Computed Tomography
NCT00474565 ·Status: WITHDRAWN ·Phase: PHASE1
-
Exploratory Pilot Study of Physical Activity Monitoring in Adult Patients With Haemophilia A by Means of Accelerometry
NCT02253693 ·Status: COMPLETED
-
The Prevalence of Radial Artery Occlusion in Diagnostic Cardiac Catheterization and Percutaneous Intervention
NCT01996553 ·Status: COMPLETED
-
Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis
NCT06218875 ·Status: RECRUITING
-
Complex Aortic Aneurysm Repair Using Physician Modified Endografts and Custom Made Devices
NCT02050113 ·Status: RECRUITING ·Phase: NA
-
Safety and Validity of Extracorporeal Fenestration and in Situ Fenestration in Patients With Aortic Disease Involving the Left Subclavian Artery
NCT06256757 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Endovascular Repair for the Descending Thoracic Aorta
NCT02376998 ·Status: COMPLETED ·Phase: NA
-
Preoperative Methylprednisolone in Endovascular Aortic Repair
NCT00989729 ·Status: COMPLETED ·Phase: NA