Clinical trial · Observational
Investigating Mechanisms to Explain Age Associated Differences in Quality of Life Among Breast Cancer Patients
NCT00582478CI-TRIAL-00116277active not recruitingClinicalTrials.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 purpose of this study is to look at how breast cancer treatment affects quality of life in women of different ages. The U.S. Army Breast Cancer Research Program funds this study. In this research project, we wish to study a woman's quality of life after breast cancer treatment as related to her health. We want to know how you feel about your quality of life.
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 |
|---|---|---|---|
| questionnaires | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- 1
- description
- women with breast cancer
- interventionNames
- Behavioral: questionnaires
Primary outcomes (1)
- measure
- The study measurements are quality of life questionnaires
- timeFrame
- 7 years 2 months
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Female * Aged 18 or older at the time of breast cancer diagnosis * English-speaking * Community dwelling (i.e. not living in a residential care or correctional facility) * Diagnosed with invasive breast cancer Stage I, II, or III within the previous 6 months * First time diagnosis * Have physician agreement for participation * Provide informed consent Exclusion Criteria: * Psychiatric or psychological abnormality precluding informed consent or ability to complete questionnaires * Previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer) * Stage IV breast malignancy * Residency outside of the United States * For women ages 45 years and younger only: Those participants \< 45 years who were having regular menstrual cycles at the time of diagnosis will be excluded from this protocol. This study will only be enrolling women in this age category who have had a prior hysterectomy or were having irregular menstrual cycles at the time of diagnosis. Women with regular menstrual cycles will be enrolled into a companion project (i.e., Menstrual Cycle Maintenance
References
Publications (0)
Data not yet available
No reference posted for this study.