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Promotion of physical activity in breast and prostate cancer survivors

Effect of a physical activity promotion program offered online or via blended care on physical activity levels in breast and prostate cancer survivors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26518
Enrollment
246
Registered
2017-12-21
Start date
2018-01-01
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

Breast and Prostate Cancer Physical Activity Fatique Mood Health related Quality of life. Borst en Prostaatkanker Fysieke activiteit Vermoeidheid Stemmingsklachten Gezondheidsgerelateerde kwaliteit van leven.

Interventions

Intervention (if applicable): IPAS consists of 6 months of noncommittal use and provides automated, algorithm-based tailored information on PA and PA assignments along with feedback on current PA leve

Sponsors

Antoni van Leeuwenhoek Rijnstate
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Histologically confirmed primary breast or prostate cancer (stages: T1 - T4, NO - N3 and M0) -Primary treatment should have been completed a minimum of 3 months and a maximum of 12 months prior to study entry. -Should not have signs of recurrence or progression at time of study entry. -Should have access to the internet in their home environment. -Should have basic proficiency in using online applications. -Should have a DIGID authentication code (to log into the program), or willing to obtain it. -Patients may currently be receiving (anti)hormonal adjuvant therapy.

Exclusion criteria

Exclusion criteria: -Patients who are unable to or cannot safely perform unsupervised exercise at the at the recommended levels. -Patients who lack basic proficiency in Dutch. -Patients who have serious cognitive or psychiatric problems that would preclude them from following the intervention or completing the study questionnaires. -Patients participating in concurrent studies or rehabilitation programs containing psychosocial and/or exercise interventions. -Patients who already meet the PA guideline of > 150 min per week of moderate to vigorous PA for longer than six months (patients in the maintenance stage according to TTM).

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is change in minutes of weekly moderate to vigorous physical activity from baseline to 6 and 12 months as assessed by accelerometer.

Secondary

MeasureTime frame
The secondary outcomes are: self-reported physical activity (IPAQ). Stage of change, fatigue (MFI) mood (POMS), HRQOL (SF-36, EQ5D) and will be assessed by questionnaires.At baseline, 6 and 12 months. Medical consumption (iMCQ) and productivity costs (iPCQ) will be measured at 6 and 12 months by questionnaire.

Contacts

Public ContactH.J. Wiel, van de
h.vd.wiel@nki.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)