Emory Universtiy
Atlanta, Georgia, 30322, United States
NCT Number: NCT01188070
More and more family members are providing care to their loved ones with prolonged and progressive illnesses. Chronic intense caregiving represents a situation of chronic stress, which takes a toll on one's mental and physical health including an increased risk for the development or worsening of heart disease. Identification of effective self-care interventions for family caregivers is warranted to improve their emotional wellbeing and minimize the harmful effects of chronic stress on the heart. This Program Project Grant aims to promote health and reduce cardiovascular risk in family caregivers (FCG) of persons with chronic illness. In two studies the investigators will test two interventions, psycho-education(ED) and physical exercise(EX), individually and in combination. The first study will target FCG of African American dementia patients; the second will focus on FCG of heart failure patients. Parallel designs, interventions and measures will create synergy as will integration of all data management and analyses within a Bio-behavioral Science and Measures Core. This Core will also provide high level guidance and interpretation of model testing resulting from analysis of the common data set. The combined de-identified data set will allow for elucidating the biological mechanisms of stress-induced cardiovascular risk, further developing the model, and stimulating future research, while the shared core support will provide substantial efficiency; neither could be achieved outside of a Program Project approach. These collective efforts will generate important data whereby future care can significantly enhance the lives of FCG and minimize their risk of cardiovascular disease, the number one cause of disability and death in the United States.
We hypothesize that FCGs who receive the combined PSYCHED+EX intervention will have better psychological functioning (lower levels of depressive symptoms, anxiety, and caregiver burden and higher levels of flourishing), behavioral outcomes (improved sleep quality and greater physical function), cardiovascular risk measures (improved resting heart rate, blood pressure, heart rate recovery, oxygen consumption, lipids, glucose, and inflammatory markers), neuroendocrine function (salivary cortisol) and overall health outcomes (improved function, muscle strength, and endurance) compared to psycho-education and usual care-attention control from baseline to six months later mediated by improvements in process outcomes (lower perceived stress and higher self-efficacy).
Looking for future studies?
Notify Me21 year and older
All sexes
Interventional
Not applicable
Atlanta, Georgia, 30322, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Educational materials
Educational group sessions
Psychoeducation intervention plus an individualized exercise program
Time frame: Baseline and 6 months
Depression, Anxiety, Caregiver Burden, Flourishing
Time frame: Baseline and 6 months
Physical Activity, Sleep Quality
Time frame: Baseline and 6 months
Function, Muscle strength, endurance
Time frame: Frame Baseline and 6 months
Salivary Cortisol
Time frame: Baseline and 6 months
Biochemical Markers (Inflammation Coagulation Insulin Resistance) Cardiovascular Reactivity & Risk
Emory University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03639402
Behavior, Cardiovascular Diseases
View Trial DetailsNCT07597460
Behavior, Child Health
Santiago, Chile
View Trial DetailsNCT04047342
Health Promotion, Wellness Programs
Danville, Pennsylvania, United States
View Trial DetailsNCT06965959
Aging, Behavior
Sivas, Central, Turkey (Türkiye)
View Trial Details