Breast cancer study probes Age-Related quality of life differences
NCT ID NCT00582478
First seen Jun 27, 2026 · Last updated Jul 01, 2026 · Updated 2 times
Summary
This study looks at how breast cancer treatment affects quality of life in women of different ages. Researchers are asking 650 women recently diagnosed with early-stage breast cancer to fill out questionnaires about their physical and emotional well-being. The goal is to understand age-related differences and improve support for all survivors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better understand and address quality-of-life issues for breast cancer survivors of all ages.
- What could go wrong
- This is an observational study using questionnaires, not a treatment trial. It may not lead to direct changes in care, and results depend on participant honesty and recall.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 650 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Oct 2001
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
First time breast cancer patients
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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