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Multidisciplinary Team IntervenTion in CArdio-ONcology (TITAN Study)

Multidisciplinary Team IntervenTion in CArdio-ONcology

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01621659
Acronym
TITAN
Enrollment
80
Registered
2012-06-18
Start date
2014-05-01
Completion date
2026-12-03
Last updated
2026-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

multidisciplinary team, exercise, nutrition, cardiology, physiotherapy, imaging

Brief summary

People with breast cancer often experience many short and long-term side effects as a result of both the cancer and the necessary treatments. Receiving extra assessments and care from teams of multiple health professionals has been shown to be helpful for people with other health problems, such as heart disease. These 'multidisciplinary' teams may include nurses, doctors, pharmacists, dietitians, exercise therapists, counselors, and other specialists. Currently, the investigators do not know if receiving extra assessments from a multidisciplinary team is helpful for people receiving cancer treatment. In this study, the investigators hope to learn the effect of extra assessments and early interventions from teams of health care professionals in people diagnosed with cancer, during and after the treatment period. After initial assessments, participants will be randomized to multidisciplinary team intervention or usual care.

Interventions

BEHAVIORALMultidisciplinary team intervention

Intervention arm receives regular assessments and treatments from cardiology team, clinical nutrition, pharmacist, exercise physiologist and physiotherapist

Sponsors

University of Alberta
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Supportive care intervention

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
cardiac MRIchange from baseline to 12 monthsleft ventricular ejection fraction (LVEF)

Secondary

MeasureTime frameDescription
serum biomarkerschange from baseline to 12 monthspercent change in established biomarkers (troponin, BNP)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 12, 2026