Skip to content

Development and Evaluation of a Cancer-Related Fatigue Patient Education Program

Development and Evaluation of a Cancer-Related Fatigue Patient Education Program

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00552552
Acronym
FIBS
Enrollment
300
Registered
2007-11-02
Start date
2008-01-31
Completion date
2009-12-31
Last updated
2007-11-02

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

Conditions

Cancer-Related Fatigue

Keywords

cancer-related fatigue, self-management, patient education, cancer survivors, chronic disease

Brief summary

The objective of this study is to develop a structured and evidence-based self-management program to cope with cancer-related fatigue and to assess the efficacy of the intervention in cancer survivors.

Detailed description

Background Cancer-related fatigue (CRF) and its impact on patients quality of life has been an increasing subject of research. However, in Germany exists a lack of evidence-based interventions consistent with the multidimensional character of fatigue. The objective of this study is to develop and evaluate a self-management program for disease-free cancer patients to cope with CRF. Methods Based on evidence extracted from a literature review a curriculum for the self-management program was elaborated. The curriculum is currently being reviewed and validated by an expert group of oncologists, psycho-oncologists, nurses, social workers, physical therapists, health scientists, and patients. The modules will be pretested with a small number of patients, discussed in terms of feasibility and acceptance. To determine the efficacy of the program a randomised controlled trial will be conducted: 300 patients will be allocated to an intervention or a waiting control group. Data will be collected before randomisation, after intervention, and after a follow-up of 6 months. Results As essential subjects for the curriculum were identified: * medical background and causes of CRF * physical activity and moderate exercise * restructuring daily schedules * energy conservation * stress-management and relaxation strategies * coping with negative emotions * integrating the new knowledge into every day life. The program aims at impacting on health-related self-efficacy by the training of problem solving, goal setting, and cognitive techniques as knowledge transfer hasn't proved sufficient to achieve changes in behaviour. According to this we developed a curriculum wherein detailed information for every module concerning objectives, background, didactic methods and materials are provided. Based on the curriculum train-the-trainer seminars are held in order to educate on moderation techniques, group dynamics, and clinical background of CRF. The program will be administered by qualified health professionals in groups of eight patients. It includes six weekly sessions 90 minutes each dealing with the topics listed above. The results of the pre-test are currently being analysed. Discussion Due to the fact that there are no comparable self-management programs for cancer survivors with fatigue the development of the curriculum has been complex. Therefore the critical appraisal by the experts was an important step to validate the program: their contributions have been integrated into the curriculum. The experts appreciated the program as filling in a gap of outpatient cancer care.

Interventions

BEHAVIORALFatigue Patient Education Program (FIBS)

6 weekly sessions, 90 min each

Sponsors

Institute of Public Health and Nursing Research (IPP)
CollaboratorUNKNOWN
German Federal Ministry of Education and Research
CollaboratorOTHER_GOV
Bremer Krebsgesellschaft e.V.
CollaboratorUNKNOWN
University of Bremen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

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

Inclusion criteria

* adult * malign neoplasms * ECOG performance status of 0-2 * moderate or severe fatigue * stable condition after treatment * German speaking

Exclusion criteria

* life expectancy \< 1 year * patients with brain neoplasms * suicidal tendencies * severe psychiatric disorders

Design outcomes

Primary

MeasureTime frame
FatigueBaseline, after the intervention, 6 months later

Secondary

MeasureTime frame
Quality of Life, Depression and anxiety, physical activityBaseline, after the intervention, 6 months later

Contacts

Primary ContactKarl Reif
karlreif@uni-bremen.de+49 421- 218
Backup ContactNina Egger
negger@uni-bremen.de+49 421- 218

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 5, 2026