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Rehabilitation of Cancer Survivors in Denmark: The Effect of a Psychosocial Rehabilitation Course

Rehabilitation of Cancer Survivors in Denmark: A Randomized Controlled Trial on the Effect of a Multi-focused Psychosocial Rehabilitation Course

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01086683
Enrollment
513
Registered
2010-03-15
Start date
2004-05-31
Completion date
2009-12-31
Last updated
2010-03-15

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

Conditions

Breast Neoplasms, Colorectal Neoplasms, Neoplasms, Prostatic Neoplasms

Keywords

neoplasms, rehabilitation, intervention, quality of life, lifestyle

Brief summary

This randomized study evaluates the effect of a multi-focused, psychosocial 6-day residential rehabilitation course at a Danish rehabilitation centre for cancer survivors. The investigators hypothesize that individuals in the intervention group will experience better psychosocial well-being and more adaptive health behaviour changes as compared to individuals in the control group.

Detailed description

Worldwide, the number of cancer survivors is increasing. In the Danish population of 5.4 million people, more than 300 000 are cancer survivors. Given the range of physical, psychological and social late effects of cancer and its primary treatment many survivors need tailored rehabilitation interventions. This randomized study evaluates the effect of a multi-focused, psychosocial 6-day residential rehabilitation course at the Dallund Rehabilitation Centre in Denmark. We hypothesize that individuals in the intervention group will experience better psychosocial well-being and more adaptive health behaviour changes as compared to individuals in the control group.

Interventions

BEHAVIORALPsychosocial rehabilitation course

Groups of 20 cancer survivors participated in a 6-day multi-focused, psychosocial intervention at the Dallund rehabilitation centre. The overall aim was to strengthen each individual's physical, psychological and social functioning. Sharing experiences with other cancer patients and experiencing peer-support was a central issue. The retreat combined lectures, discussions and patient group work on themes such as the treatment of cancer, psychological reactions, spirituality, sexuality and lifestyle. Participants were involved in physical activities, and the daily menu represented a healthy diet. The course was conducted by a multi-disciplinary team. Each participant produced a personal, specific 'action plan', which was intended to serve as a 'booster' after returning to daily life.

Sponsors

University Hospital Århus, Department of Surgery
CollaboratorUNKNOWN
University Hospital Århus, Urology Department
CollaboratorUNKNOWN
Randers Regional Hospital
CollaboratorOTHER
Regional Hospital Hørsholm, Department of Breast Surgery
CollaboratorUNKNOWN
Danish Cancer Society
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Diagnosis of breast, colorectal or prostate cancer * Completion of primary treatment * Ability to participate physically in the activities offered in the intervention

Exclusion criteria

* Acute need for treatment * Terminal cancer phase

Design outcomes

Primary

MeasureTime frameDescription
psychosocial well-being (as assessed by the EORTC-QLQ C30 Quality of life core questionnaire by the European Organization of Research and Treatment in Cancer (EORTC-QLQ C30) and the Profile of Mood States Short form (POMS-SF)baseline, 1 month follow-up, 6 month follow-up, 12 month follow-upself-report questionnaire

Secondary

MeasureTime frameDescription
health behaviours: physical activity, diet, tobacco and alcohol consumption, use of health servicesbaseline, 1 month, 6 month, 12 month follow-upself-report questionnaire
self-rated healthbaseline, 1 month, 6 month, 12 month follow-upself-report item
self-efficacy as measured with the General Self-Efficacy Scale (GSE)baseline, 1 month, 6 month, 12 month follow-upself-report questionnaire

Countries

Denmark

Outcome results

None listed

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