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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01060761
Other study ID # HMS-SDU- 2009-1
Secondary ID
Status Completed
Phase N/A
First received February 1, 2010
Last updated November 2, 2017
Start date March 2010
Est. completion date December 2011

Study information

Verified date June 2012
Source University of Southern Denmark
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective is to investigate a rehabilitation program (supportive conversations and a rehabilitation course for cancer patients and their relatives together).

The study evaluate the effect of the program compared to no intervention (usual care)


Description:

The study aim to evaluate the effect and the benefit of the program.

First the patients psychosocial well-being is assessed in a survey (EORTC, POMS, WHO-5 well-being index) Then their relatives psychosocial well-being is assessed in a survey (Ad hoc questions, POMS and WHO-5 well-being index)

The effect is also assessed in qualitative interviews with patients and their relatives.

The rehabilitation course is investigated in qualitative observations and interviews.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date December 2011
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Both the patient and their relative must agree to participate together

- Patient admitted to the Hospital

- Patient admitted with a lung cancer diagnosis or

- Patient admitted with a gynecological cancer diagnosis

Exclusion Criteria:

- The cancer diagnosis was not verified.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Rehabilitation program
Patient and their relative receive three supportive, structured conversation with a trained nurse. Patient and their relative receive 4 days Retreat Weekend with supportive talk and activities

Locations

Country Name City State
Denmark Odense University Hospital Odense

Sponsors (2)

Lead Sponsor Collaborator
University of Southern Denmark Odense University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of life, two months and one year
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