Clinical trial · Observational
A Qualitative Study on Advanced Breast Cancer Patients and Their Caregivers in Spain
Ethnographic Study on Advanced Breast Cancer Patients and Their Caregivers in Spain
NCT06683482CI-TRIAL-00093164completedClinicalTrials.gov clinicaltrialsProvenance
- 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)
The main goal of this ethnographic study is to learn a holistic and enriched view of the behaviors, actions, and views of a group of people with advanced breast cancer (ABC) cancer living in Spain. The primary objective of this study is to collect data on the psychosocial needs of (ABC) patients to identify spaces and strategies to improve these needs.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| No intervention | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Participants with Advanced Breast Cancer Living in Spain and their Caregivers
- description
- Participants with different types of breast cancers living in Spain will be observed in this study. Participants will not receive any study drug in this study.
- interventionNames
- Other: No intervention
Primary outcomes (1)
- measure
- Number of Participants With Responses to the Open-ended questionnaires
- timeFrame
- Up to 4 weeks
- description
- This qualitative ethnographic study will be carried out through the transcriptions of open-ended interviews. The variables of interest will consist of a set of sociodemographic data, as well as results from emotional and psychological.
Secondary outcomes (5)
- measure
- Number of Participants with Responses to the Open-ended Questionnaires Related to Intimacy and Sexuality
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Key Inclusion Criteria: 1. Informed consent to individual in the qualitative study and to allow the recording of the interview for analyses purposes (individual and/or caregiver). 2. Women or men (individual and/or caregiver) over 18 years of age. 3. Confirmed diagnosis of triple-negative breast cancer (TNBC), hormone receptor (HR)+/ human epidermal growth factor receptor 2 (HER2)-, HER2+ unresectable locally advanced breast cancer (ULABC) or metastatic breast cancer (mBC) (individual). 4. Individuals must have initiated at least the firstline treatment. 5. Functional status according to the Eastern Cooperative Oncology Group (ECOG) scale 0-2 (individual). 6. Ability to conduct interviews from home (individual and/or caregiver) or remotely (ie, with technology available for an online interview). Key Exclusion Criteria: 1. Individual unable to collaborate in the collection of necessary information (alteration in mental status, noncollaboration, limited language comprehension). 2. Individual unable or unwilling to provide informed consent. Note: Other protocol defined Inclusion/Exclusion criteria may apply
References
Publications (0)
Data not yet available
No reference posted for this study.