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Putting the patient at the center of care: personalized treatment for psychological symptoms and fatigue in cancer survivors

Putting the patient at the center of care: personalized treatment for psychological symptoms and fatigue in cancer survivors - MATCH

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON55738
Enrollment
190
Registered
2019-01-15
Start date
2019-02-13
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

angst, depressieve symptomen en vermoeidheid na kanker depressive symptoms and fatigue after cancer fear of cancer recurrence

Interventions

Personalized treatment group: Psychological treatment will be systematically tailored on four levels: 1. Treatment indication: most studies select patients based on their symptom level. A patient*s
identification of patients* most burdensome symptom). Following the standard protocols of the treatment for fear

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a patient must meet all of the following criteria: 1) be >=18 years old; 2) be able to speak and read Dutch; 3) be diagnosed with a cancer diagnosis; 4) be at least six months and maximum 5 years after end of primary treatment with curative intent; 5) have no disease activity at time of inclusion in the study; 6) report either clinical relevant levels of fatigue (Checklist Individual Strength (CIS), cutoff >= 35 on the fatigue severity subscale), and/or fear of cancer recurrence (Cancer Worry Scale (CWS, 6-item), cutoff >= 10) and/or depressive symptoms (Beck Depression Inventory Primary Care (BDI-PC), cutoff >= 4), and must experience functional impairments (Work and Social Adjustment Scale (W&SAS), cutoff >=10 [22,23]); 7) in case of fatigue: be determined by their physician to have no clinical condition or disease that could account for their fatigue presentation.

Exclusion criteria

Exclusion criteria: Insufficient command of the Dutch language, currently receiving psychological or psychiatric treatment, no informed consent.

Design outcomes

Primary

MeasureTime frame
Primary outcome is patient functioning (questionnaire: Sickness Impact Profile-8 (SIP-8)).

Secondary

MeasureTime frame
Secondary outcomes are symptom level (fear or cancer recurrence (Cancer Worry Scale, CWS), depression (Beck Depression Inventory for Primary Care, BDI-PC), and fatigue (Checklist Individual Strength, CIS), quality of life (EORTC QLQ-C30 questionnaire), and goal attainment (Goal Attainment Scaling (GAS).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)