Clinical trial · Observational
Frequency of Cachexia in Ambulatory Cancer Patients and Psychological Burden in Patients and Their Primary Caregivers
Frequency of Cachexia in Ambulatory Cancer Patients and Psychological Burden in Both Patients and Their Primary Caregivers Who Are Referred to an Outpatient Supportive Care Clinic
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This trial studies the frequency of cachexia in ambulatory cancer patients and the psychological burden in patients and their primary caregivers who are referred to an outpatient supportive care clinic. Studying how often loss of appetite and/or unintentional weight loss (cachexia) occurs in patients seen in the supportive care clinic may help researchers develop new ways to lower stress in patients who suffer from loss of appetite and weight loss as well as their family caregivers.
Conditions
Conditions (7)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Advanced Malignant Solid Neoplasm | Malignant Solid Neoplasm | CURATED_BROADER | 0.78 |
| Caregiver | — | UNRESOLVED | — |
| Metastatic Malignant Solid Neoplasm | Malignant Solid Neoplasm | CURATED_BROADER | 0.78 |
| Recurrent Leukemia | Leukemia | CURATED_BROADER | 0.78 |
| Recurrent Lymphoma | Lymphoma | CURATED_BROADER | 0.78 |
| Recurrent Malignant Solid Neoplasm | Malignant Solid Neoplasm | CURATED_BROADER | 0.78 |
| Recurrent Plasma Cell Myeloma | Multiple Myeloma | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Questionnaire Administration | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Observational (questionnaires)
- description
- Participants complete 8 questionnaires about appetite, quality of life, symptoms, history of weight loss, nutritional status, body image, and nutritional support over 30 minutes.
- interventionNames
- Other: Questionnaire Administration
Primary outcomes (1)
- measure
- Cancer Cachexia
- timeFrame
- Day 1
- description
- Assessed by either European Society for Clinical Nutrition and Metabolism (ESPEN) includes body mass index (BMI) \< 18.5 (mandatory) or combined finding of unintentional weight loss (mandatory) and at least one of either reduced BMI or a low fat free mass index (FFMI), or International Consensus Criteria (ICC) defined as cachexia weight loss greater than 5% over 6 month period or weight loss greater than 2% showing depletion according to current bodyweight and height over an indefinite time point.
Secondary outcomes (8)
- measure
- Functional Assessment of Anorexia Therapy-Anorexia/Cachexia Subscale Questionnaire (FAACT-A/CS)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. \[Patient\] Patients visiting the Supportive Care Clinic (SCC) for a consultation or a follow up. 2. \[Patient\] Patients who can identify a primary caregiver. 3. \[Patient\] Diagnosis of advanced cancer defined as locally advanced, recurrent, or metastatic. 4. \[Patient\] Be able to read and speak English. 5. \[Patient\] 18 years of age or older. 6. \[Caregiver\] Be identified or self-identified as a primary caregiver of the patient. 7. \[Caregiver\] Provide informed consent 8. \[Caregiver\] Be able to read and speak English. 9. \[Caregiver\] 18 years of age or older. 10. \[Caregiver\] Caregivers who are not able to complete the questionnaire on the day of patients' SCC visit must be willing to engage in a telephone questionnaire with research staff within 60 days of the patient's enrollment. Exclusion Criteria: 1. \[Patient\] Refusal to participate in this study. This study requires both patient and caregiver enrollment. 2. \[Patient\] Patients with no caregiver or only paid caregivers. 3. \[Patient\] Patients with cognitive impairment as identified by research staff, treating physician or nurse (Memorial Delirium Assessment Scale score of \>/= 7). 4. \[Caregiver\] Refusal to participate in this study. This study requires both patient and caregiver enrollment. 5. \[Caregiver\] Not a primary caregiver or is a paid caregiver. 6. \[Caregiver\] Evidence of cognitive impairment, as determined based on orientation questions pertaining to the date, day of the week, time, and place
References
Publications (0)
Data not yet available