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Clinical Trial Summary

To investigate the effects of patient counseling by telephone on Quality of Life and the use of Health care system.


Clinical Trial Description

By analyzing patient data, patients with risk of high consumption of the Health system are identified.

These patients are invited to take part in the study. If the patient accept the invitation, oral and written information of the study is given. If the patient give informed consent to participate, the inclusion and exclusion criteria and the patient record are examined.

If the patient meet the criteria the patient is randomized to active treatment or control 1:1.

Patient in the Intervention Group have a in depth interview of Health and social status and possible interventions are planned. Following that, the patient is contacted by telephone on weekly intervals for 6 to 9 months.

Patients in both Groups fill out questionaire Short-Form Health Survey-36 (SF-36) and COPD Assessment Test (COPD) and the consumption of Health care is monitored. ;


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT02457533
Study type Interventional
Source Region Sjælland
Contact Knud Rasmussen, MD DMSci
Phone +45 60168891
Email kra@regionsjaelland.dk
Status Recruiting
Phase N/A
Start date April 2015
Completion date April 2016

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