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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05341440
Other study ID # 27122021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 22, 2022
Est. completion date June 22, 2024

Study information

Verified date February 2023
Source Bar-Ilan University, Israel
Contact Jenny Gutman
Phone 0547851988
Email jenny.e.gutman@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The established attachment theory elucidates how early human bonds bring about functional neurophysiological alterations influencing the lifelong capacity for self and co- regulation within relationships. Based on this framework, the study will investigate potential psycho-physiological co-regulation processes in couples coping with cardiovascular disease, which may explain the established link between relationship satisfaction and recovery outcomes. In the proposed prospective, longitudinal study, the investigators will follow 81 volunteer couples in which one member has experienced an Acute Coronary Syndrome and assess their levels of interactive behavioral synchrony and the accompanying physiological synchrony (the mutual coordination of spouses' autonomic nervous systems), and stress buffering (reduced reactivity to stress in the individual) as assessed by Heart Rate Variability, and Galvanic Skin Response. It is hypothesized that higher levels of physiological synchrony and stress buffering will be associated with enhanced behavioral synchrony in the lab as well as patient outcomes three months later, on three dimensions: emotional (anxiety and depression reduction); behavioral (smoking cessation, medication adherence, cardiac rehabilitation participation) and physical (weight reduction, increased fitness).


Recruitment information / eligibility

Status Recruiting
Enrollment 81
Est. completion date June 22, 2024
Est. primary completion date March 22, 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - First Acute Coronary Syndrome - In a committed relationship lasting over a year - Registration at the Cardiac Prevention and Rehabiliation Center (CPRC) Exclusion Criteria: - A history of previous cardiac events - A diagnosis other than Acute Coronary Syndrome, co-morbid conditions (such as cancer), - Lack of Hebrew as a native language. - Exclusion criteria for partners will be severe co-morbid conditions with life expectancy of less than 6 months (such as advanced cancer) and lack of Hebrew as a native language.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba Medical Center Ramat Gan Hamercaz

Sponsors (1)

Lead Sponsor Collaborator
Bar-Ilan University, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hospital Anxiety and Depression Scale contains 14 items and consists of two subscales: anxiety and depression. Each item is rated on a four-point scale, giving maximum scores of 21 for anxiety and depression. Scores of 11 or more on either subscale are considered to be a significant 'case' of psychological morbidity, while scores of 8-10 represents 'borderline' and 0-7 'normal'. 3 months
Primary The Warwich-Edinburgh Mental Well-being Scale A scale of 14 positively worded items for assessing a population's mental wellbeing. Scores range from 14 to 70 and higher scores indicate greater positive mental wellbeing. 3 months
Primary Smoking cessation Smoking cessation will be defined as the delta between the number of cigarettes smoked before the cardiac event and the number of cigarettes smoked 3 months after the start of rehabilitation. 3 months
Primary The Medication Adherence Report Scale Patients will be asked to report on their medication adherence, using the Medication Adherence Rating Scale. Responses are summed for a total score ranging between 5 and 25, with higher scores indicating a higher level of adherence. 3 months
Primary Cardiac rehabilitation participation The number of times patients participated in supervised exercise in the Cardiac Rehabilitation Center. Information regarding Rehabilitation participation will be retrieved from patients' computerized entry files. 3 months
Primary Weight change Weight change is defined as the delta between patients' body-mass index (BMI) from the beginning of rehabilitation and 3 months in. 3 months
Primary Fitness change Will be defined as the change in delta between 3 months after the start of rehabilitation ergometry score and the start of rehabilitation ergometry score (in Metabolic Equivalent of Task Score- METs). 3 months
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