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Lifestyle change, self-management, and problem solving in daily life in cancer survivors; an online portal for change and support.

The effectiveness and evaluation of an online cancer aftercare intervention concerning lifestyle change, self-management, and problem solving in cancer survivors.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29153
Enrollment
800
Registered
2012-03-29
Start date
2013-10-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Tertiary Prevention, Cancer survivors, Cancer Aftercare, Disease self-management, Social support, Lifestyle, Quality of life, Psychosocial distress.

Interventions

Cancer survivors in the experimental group who enter the online portal receive general information on dealing with distress, obtaining social support, disease self-management, and optimizing healthy l

Sponsors

Open University of the Netherlands, Maastricht University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. 18 years of age or older; 2. Patients who were previously diagnosed with cancer; 3. Successful completion of the main treatment period, up to one year ago; 4. People who receive aftercare (e.g., preventive hormonal therapy) or medical check-ups are allowed to participate; 5. No cancer during last medical check-up; 6. Patients with all types of cancer are allowed to participate; no groups are excluded (on condition that the main treatment period is successfully completed); 7. Ability to speak and read the Dutch language; 8. Access to the web and minimal internet experience (monthly access).

Exclusion criteria

Exclusion criteria: Patients with a serious medical, psychiatric, or cognitive disease that would interfere with participation.

Design outcomes

Primary

MeasureTime frame
1. The extent of psychosocial distress; 2. Health related quality of life in patients. Psychosocial distress will be measured with the General Health Questionnaire – 12 item version (GHQ-12) and the Hospital Anxiety and Depression Scale (HADS). Quality of life will be measured with the European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire (EORTC QLQ-C30). Both primary outcomes will be assessed at all time points.

Secondary

MeasureTime frame
1. Lifestyle behaviors; 2. Coping behaviors; 3. Self-management & problem solving behaviors; 4. Empowerment; 5. Perceived social support. Physical activity will be measured with the SQUASH; a validated physical activity measure. Smoking behavior will be measured with a validated 7-days recall questionnaire. Alcohol consumption will be measured with a standardized scale to assess the amount of alcohol consumption. Dietary behaviors will be measured by validated food frequency questionnaires on respectively saturated fat-intake and vegetable and fruit consumption. Habit strength will be measured by means of the Self-Report Habit Strength Index. Self management is operationalized as problem-solving. It will be measured using the SPSI-R, a self-report questionnaire. Empowerment will be measured with a short validated questionnaire. The questionnaire will be adapted for the specific situation of cancer survivors. Perceived social support will be measured with the SSL-I. Perceived peer support will be measured with SSL-D and SSL-I subscales that will be developed for the purpose of the study. All secondary outcomes will be assessed at all time points.

Contacts

Public ContactLinda Küsters

PO Box 2960 Chiba 3.21

linda.kusters@ou.nl+31 (0)45 5762448

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)