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Involvement of Patients and Relatives in the Course of Cancer Disease

Involvement of Patients and Relatives in the Course of Cancer Disease With a Particular View to Rehabilitation and the Life With Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01060761
Acronym
KRIPP
Enrollment
42
Registered
2010-02-02
Start date
2010-03-31
Completion date
2011-12-31
Last updated
2017-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Rehabilitation, Relatives

Keywords

cancer, Rehabilitation program (patient and a relative together), counselling, retreat weekend

Brief 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)

Detailed 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.

Interventions

BEHAVIORALRehabilitation 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

Sponsors

Odense University Hospital
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Quality of life,two months and one year

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026