Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
130 participants
OBSERVATIONAL
2011-04-30
2014-12-31
Brief Summary
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Detailed Description
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The current research aims to broaden the understanding of spousal support among couples coping with a life threatening illness- Coronary Heart Disease (CHD) versus general population of couples. Two studies were designed. Study 1(control group) will focus on general population of couples and its goal is examine the contribution of personality traits of the couples to their marital satisfaction and well-being. Study 2 (target group) will focus on couples coping with a first acute coronary heart disease and its goal is to examine the contribution of personality traits of the couples to their marital satisfaction and well-being, and to health promoting behaviors (smoking cessation, medication adherence) and physical recovery (change in body mass index, change in cholesterol levels) of the ill partners.
The proposed research is a prospective, longitudinal study. The control group will be 100 couples who are not coping with a life threatening illness. The couples will complete self report questionnaires. The target group will be 127 male patients and their partners. The couples will be recruited during the patients' first hospitalization for ACS. The participants will complete questionnaires during the hospitalization and again six months later. Relevant data will be obtained from their medical files.
This study's findings could inform clinicians whose goal is to foster better patient-spouse dynamics in the context of major medical stressors. Helping couples master the challenge of providing and receiving support in such trying times may contribute to enhanced levels of adherence among patients which, in turn, would lead to improved health and saved lives.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Couples coping with CHD
The target group will be 127 male patients and their partners. The couples will be recruited during the patients' first hospitalization for ACS. The participants will complete questionnaires during the hospitalization and again six months later. The patients will also be asked to be weighed and have their blood drawn and at the six-month follow-up for measurement of blood Cholesterol level. Relevant data will be obtained from their medical files.
No interventions assigned to this group
control group
The control group will be 100 couples who are not coping with a life threatening illness. The couples will complete self report questionnaires at one point of time.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Partners also agree to participate in the study
Exclusion Criteria
* a diagnosis other than ACS
* co-morbid conditions (such as a severe psychiatric illness, end state renal disease or severe cancer)
* absence of a spouse
* inability to be interviewed in Hebrew
ALL
Yes
Sponsors
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Meir Medical Center
OTHER
Responsible Party
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Principal Investigators
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Morris Mosseri, Professor
Role: PRINCIPAL_INVESTIGATOR
Department of Cardiology, Meir Medical Center, Israel
Locations
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Department of Cardiology, Meir Medical Center
Kfar Saba, , Israel
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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MMC10psycho-cardioCTIL
Identifier Type: -
Identifier Source: org_study_id
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