Female genital neoplasms: cervical-, vulvar-, endometrial- or vaginal cancer Malnutrition Sarcopenia
Conditions
Interventions
No interventions occur, study procedures only include additional measurements.
Sponsors
Amsterdam UMC, location AMC
Eligibility
Inclusion criteria
Inclusion criteria: • Aged = 18 years • Scheduled for EBRT with curative intent for histologically confirmed cervical-, endometrial-, vulvar-, or vaginal cancer • Written informed consent
Exclusion criteria
Exclusion criteria: • Inability to read and write Dutch
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference fat free mass percentage point as measured by CT-scan between baseline and the six-month of follow up. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Social participation (recovery) measured by PROMIS questionnaire: ability to participate in social roles and activities v2.0 Short form 8a. • Nutritional status and gastrointestinal symptoms will be assessed by: Data collection part of standard of care: - Body mass index (BMI) - Short Nutritional Assessment Questionnaire (SNAQ)-score - Gastro-intestinal symptoms (EORTC-C30 and CX-24) - Gastro-intestinal morbidity (CTCAE v5.0 rectum/sigmoid and colon/bowel) Data collection part of study procedures: - Fat free mass and fat mass (Bio-elektrische Impedantie Analyse; BIA) - Mid-arm muscle circumference incl. skinfold measurement (muscle mass and percentage) • Dietetic care will be evaluated by: - Referral rates to dietary care. - Waiting time for dietary care. - Percentage of patients who withdraw from nutritional care. - Reasons for withdraw from dietetic care by qualitative assessment of reasons for withdraw from nutritional care will be performed. | — |
Contacts
Public ContactJanna Laan
Amsterdam UMC, locatie AMC
Outcome results
None listed