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PanCareFollowUp: Feasibility of a person-centred eHealth intervention for survivors of childhood, adolescence, and young adult cancer

PanCareFollowUp: Feasibility of a person-centred eHealth intervention for survivors of childhood, adolescence, and young adult cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28694
Enrollment
60
Registered
2020-09-29
Start date
2020-11-01
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

Late effects in survivors of childhood cancer

Interventions

The PanCareFollowUp Lifestyle intervention consists of an intake session and 3 to 6 screen-to-screen video-coaching sessions via a secure internet connection within a period of 3-4 months. Four months

Sponsors

Radboud University Medical Center, Nijmegen, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: To be eligible for the PanCareFollowUp Lifestyle intervention, a survivor must: 1. be a survivor of childhood, adolescent or young-adult cancer survivor (diagnosed with any type of cancer under the age of 25); 2. be at least 5 years from end of treatment; 3. be cancer free; 4. be aged 16-55 years at time of intervention; 5. have at least one of the following unhealthy lifestyle behaviours defined as; - not meeting the World Health Organization norm for physical activity (exercising at least 150 minutes of moderate-intensity aerobic physical activity throughout the week or do at least 75 minutes of vigorous-intensity aerobic physical activity throughout the week or an equivalent combination of moderate- and vigorous-intensity activity): - unhealthy dietary intake manifested by overweight (BMI = 25 kg/m2). 6. be motivated to change their unhealthy lifestyle behaviour(s).

Exclusion criteria

Exclusion criteria: 1. diagnosed with Down syndrome; 2. diagnosed with cognitive disorders; 3. has depressive symptoms (H.A.D.S. total score =11 and anxiety and depression subscore =8); 4. currently receiving treatment for secondary malignancies; 5. diagnosed with endocrine disorders (with the exception of Type II Diabetes and/or hyperthyroid for which the survivor is treated) or other conditions that limit the survivor’s ability to engage in health promotion discussions and activities 6. Has underweight (BMI = 20 kg/m2), as survivors with underweight need a different and multidisciplinary intervention.

Design outcomes

Primary

MeasureTime frame
The main study endpoint of the PanCareFollowUp Lifestyle intervention will be the percentage of survivors that improve their lifestyle on the behaviour(s) that they desire to change, i.e. the goals that were set with the coach.

Secondary

MeasureTime frame
Secondary endpoints are changes in physical activity level, dietary intake, BMI, motivation level, self-reported empowerment and costs. Secondary endpoints regarding feasibility outcomes evaluation of the PanCareFollowUp Lifestyle intervention will be determined through a number of indices assessed with questionnaires and with nurses’ reports: (i) adherence CAYA survivors with intervention (compliance); (ii) acceptability (satisfaction with content, delivery and time load); (iii) practicality satisfaction mode of delivery); (iv) integration/implementation of the interventions (facilitators/barriers, success/failure goals). The secondary endpoint regarding to cost benefit evaluation will be the cost benefit ratio of the PanCareFollowUp Lifestyle intervention.

Contacts

Public ContactLeontien Kremer

Princess Máxima Center

l.c.m.kremer@prinsesmaximacentrum.nl088 972 7272

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)