CClinicalTrials.gg
Status unknownNCT01589536SINKOUpdated May 2, 2012

Social Medical Progression of Coronary Heart Disease With Associated Psychosocial Comorbidity -Interval Rehabilitation.

An interventional study of interval-rehabilitation in Cardiovascular Events, sponsored by Clinic Roderbirken. Status unknown at 1 site in Germany. Open to participants aged 18 Years to 58 Years. Per ClinicalTrials.gov, last updated 2012-05-02.

Sponsored by Clinic Roderbirken · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Apr 2012), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
480
Allocation
Randomized
Ages
18 Years to 58 Years
Sex
All
01

Study summary

The purpose of the study is to verfiy the hypothesis if a short intensive psychocardiological interval-intervention, combined with a structured follow up, decreases the rate of disability retirements caused by psychosocial co-morbidity of patients with coronary heart disease.

Read the detailed description

The purpose of the study is to verfiy the hypothesis if a short intensive psychocardiological interval intervention, combined with a structured follow up, decreases the rate of disability retirements caused by psychosocial co-morbidity of patients with coronary heart disease.

02

Conditions studied

  • Cardiovascular Events

Keywords

  • psychocardiological
  • interval intervention
  • disability pension
  • risk profile
  • mental comorbidity
03

In context

Heart Diseases

3,639 studies on the registry are indexed under Heart Diseases; 461 are open to participants now.

This study's planned enrollment of 480 is above the median of 100 across 1,778 interventional studies indexed under Heart Diseases.

Browse Heart Diseases studies →

Lead sponsor

This is the only study on the registry with Clinic Roderbirken as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 58 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Coronary heart disease
  • Disease-related psychosocial morbidity
  • not a disability retirements
  • Insured with the German Rheinland pension (deutsche Rentenversicherung Rheinland)
  • Sufficient language skills
  • Age 18-58

Exclusion criteria

Exclusion Criteria:

  • Acute cardiac decompensation
  • consuming the underlying disease
  • psychotic disorder
  • Acute suicidality
  • pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
480 participants (estimated)

Study arms

  • Experimental
    Interventiongroup

    A Stationary psychocardiological interval-rehabilitation.

    Other: interval-rehabilitation

  • No intervention
    controlgroup

    The Patients in the control group receive a personal recommendation concerning psychotherapy outpatient counseling and therapy services at home and take therapeutic help.

Interventions

  • Otherinterval-rehabilitation

    The Patients in the intervention group receive a Stationary psychocardiological interval-rehabilitation.The Interval rehabilitation is divided into individual psychological therapy with focus of Behavior therapy and relaxation therapy.

    Also known as: psychocardiological, interval rehabilitation, Roderbirken, comorbidity, sarah

06

What researchers measure

Primary outcomes

  1. Improvement of the social medical progression of coronary heart disease with associated psychosocial comorbidity by the use of interval rehabilitaion

    Reducing the rate of disability pension of 18%of 9% by interval-rehabilitation with aftercare.

    Time frame: 24 months after including study

Secondary outcomes

  1. Improvement of the social medical progression of coronary heart disease with associated psychosocial comorbidity by the use of interval rehabilitaion

    Reduction of cardiovascular events, including deaths Improving the risk profile Improvement of health-related quality of life Improvement of mental comorbidity

    Time frame: 24 months after including study

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 2, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01589536
Lead sponsor
Clinic Roderbirken
Responsible party
Sponsor
First posted
May 2, 2012
Start date
Oct 2011
Primary completion
Dec 2015 (estimated)
Completion
Dec 2016 (estimated)
Last update
May 2, 2012

Study contacts

Wolfgang Mayer-Berger, MD
principal investigator · Clinic Roderbirken

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

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