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NCT02360189 Clinical Trial

Mechanisms of Social Inequalities in Post-hospitalization Rehabilitation in Patients With Acute Coronary Syndrome

Acute Coronary Syndrome Clinical Trial

Official title:
Mechanisms of Social Inequalities in Post-hospitalization Rehabilitation in Patients With Acute Coronary Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02360189
Other study ID # ACS-12345
Secondary ID
Status Completed
Phase
First received November 26, 2014
Last updated March 28, 2018
Start date March 2015
Est. completion date March 2018

Study information
Verified date March 2018
Source Nordsjaellands Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Aim: To identify psychological and socioeconomic predictors of cardiac-rehabilitation (CR) attendance and uncover mechanisms of CR non-attendance.

Design: Quantitative, observational, prospective study. Hypothesis a: Educational-level, comorbidity, anxiety, depression, self-efficacy, cohabitation and distance from residence are predictors of CR attendance.

Hypothesis b: The expected social gradient in CR attendance is explained partly by differential exposure of comorbidity, anxiety, depression, self-efficacy, cohabitation and distance to the rehabilitation clinic.

Description:

Design: Quantitative, observational, prospective study. Self-administrated questionnaires, medical journals and telephone interviews will be used for data collecting.

Recruitment information / eligibility
Status Completed
Enrollment 310
Est. completion date March 2018
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients hospitalized with acute coronary syndrome (ACS) to Nordsjællands Hospital (ICD10: DI210-DI219, DI200, DI200B, DI200C, DI23, DI24) will be invited to participate in the survey as an ongoing process during the inclusion period (N=267).

Exclusion Criteria:

- Patients who are not able to submit written consent are excluded. Thus, patients with severe cognitive dysfunction or poor language skills are excluded.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Denmark Nordsjællands Hospital, Frederikssund. Frederikssund
Denmark Nordsjællands Hospital, Hillerød Hillerød

Sponsors (1)
Lead Sponsor Collaborator
Nordsjaellands Hospital

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cardiac-rehabilitation attendance (yes/no) 3 months post hospitalization
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