Heart-Smart cancer care: team approach tested in breast cancer patients
NCT ID NCT01621659
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether extra care from a team of heart doctors, dietitians, exercise therapists, pharmacists, and physiotherapists can reduce side effects in breast cancer patients receiving chemotherapy. About 80 participants will be randomly assigned to either the team intervention or usual care. The main goal is to see if this approach helps preserve heart function during and after cancer treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- multidisciplinary team intervention (cardiology, nutrition, exercise, pharmacy, physiotherapy assessments and counseling)
- What this could lead to
- If it works, this could show that extra support from multiple health experts reduces heart damage and improves quality of life during and after cancer treatment.
- What could go wrong
- This is a small, early-phase study with only 80 participants, so results may not apply to everyone. The extra care may not significantly improve outcomes over usual care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
80 people
The number who actually took part.
- Start date
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May 2014
- Expected to finish
-
Dec 2026
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.
- Ages
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18 years and older
- Sex
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Anyone
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * histologically confirmed malignancy (breast or lymphoma); * scheduled to receive anthracycline and/or trastuzumab-based chemotherapy; * age ≥ 18 years; * willing to attend follow-up visits. Exclusion Criteria: * physical disability preventing exercise testing or DEXA scan; * psychiatric disease or disorder precluding informed consent; * participation in other cardiotoxicity or exercise intervention study; * contraindication to anti-cancer therapy, including known heart failure, cardiomyopathy, or baseline LVEF \< 50%; * previous anthracycline or trastuzumab-based therapy; * previous radiotherapy to thorax.
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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
-
Cross Cancer Institute
Edmonton, Alberta, T6G 1Z2, Canada
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