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Randomized Trial of Behavioral Intervention Versus Standard Treatment

NCT00888485 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 362

Last updated 2009-04-27

No results posted yet for this study

Summary

The purpose of this study is to determine the possible preventive effect of behavioural modification versus standard treatment after hospital discharge in CHD patients.

Conditions

Interventions

BEHAVIORAL

Behavioral interventional program

Cognitive behavioral therapy intervention adapted to coronary disease patients performed in 20 group sessions during one year.

Sponsors & Collaborators

  • Uppsala University

    lead OTHER

Principal Investigators

  • Kurt Svärdsudd, MD PhD · Uppsala University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1996-05-31
Primary Completion
2008-12-31
Completion
2008-12-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00888485 on ClinicalTrials.gov