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Early-Stage Breast CancerNCT00233077

Patient Centered Randomized Controlled Trial

A study testing Patient Assistance and Information only in people with Early-Stage Breast Cancer, run by Icahn School of Medicine at Mount Sinai at 8 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to determine whether patient-assistance programs as compared with usual care will help women with early stage breast cancer receive appropriate treatments. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Early-Stage Breast Cancer
What is being tested?
Patient Assistance and Information only
Could I receive a placebo?
No, everyone receives an active treatment
How many people
374 participants
Where
8 sitesUnited States
Study dates
Oct 2006to Jan 2011
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • All patients, who are English or Spanish speaking, with a new primary stage 1 or 2 breast cancer who have undergone either breast conserving surgery or mastectomy and those with tumors >1cm or <1cm and poorly differentiated;
  • All surgeons performing breast surgery at the participating hospitals

Who cannot join

  • Patients with dementia or those with a poor prognosis due to end-stage organ failure or other concomitant conditions such as those undergoing treatment for other cancers

Trial locations and contacts

8 sites in 1 country.

8 sites in 1 country

United States8 sites
  • Icahn School of Medicine at Mount Sinai

    New York, New York, 10029

  • Metropolitan Hospital

    New York, New York, 10029

  • Columbia University

    New York, New York, 10032

  • Harlem Hospital Center

    New York, New York, 10037

  • Albert Einstein College of Medicine

    New York, New York, 10461

  • Montefiore Medical Center

    New York, New York, 10467

  • Elmhurst Hospital Center

    Queens, New York, 11373

  • Queens Hospital Center

    Queens, New York, 11432

Other trials in United States

About this study

Official title: Patient Assistance to Reduce Breast Cancer Disparities

The purpose of this study is to determine whether patient-assistance programs as compared with usual care will help women with early stage breast cancer receive appropriate treatments.

Read the detailed description

Numerous trials proved the efficacy of radiation following breast conserving surgery and systemic therapies to increase disease-free and overall survival among women with early-stage breast cancer. Yet 14%-89% of women do not receive them, especially minority women. Despite lower incidence of the disease, African American women are more likely than white women to die of breast cancer. As we near racial equity in rates of breast cancer screening, disparities in treatment and mortality remain. Efforts to achieve control of breast cancer and reduce racial disparities in mortality will not be fully realized until proven effective treatments are provided to those who can benefit.

Underuse of effective treatments may be caused by patient, physician and system factors. For breast cancer screening, women's lack of access to care; insurance; transportation; beliefs about fatalism and curability, and cancer's effect on partner relationships, all impact mammography rates. For breast cancer treatment, little is known about patient-related reasons for underuse, and less is known about racial differences in such reasons.

Interventions targeted to specific causes are more likely to succeed. For breast cancer screening, patient-centered interventions that successfully raise mammography rates among minority women include lay health workers to raise awareness about and address cultural beliefs and barriers to screening, vouchers to pay for screening and navigators to help women with abnormal screenings obtain needed follow-up. For breast cancer treatment, patient-assistance programs provide practical support such as financial counseling, aid with navigating the complex healthcare system, emotional support, and information about cancer and its treatment. Such programs abound but patients are often unaware of them. While these services may increase the receipt of effective adjuvant therapies, these strategies have not been rigorously tested.

We propose to conduct a randomized controlled trial to evaluate the effectiveness of patient-assistance programs as compared with usual care on receipt of adjuvant therapies among minority and nonminority women with newly operated early-stage breast cancer. During the 24 month trial, we will assess patients' beliefs about cancer and its treatment, and their practical, psychosocial, and informational needs and barriers to care. We will identify and train employees in existing cancer assistance services in order to increase the sustainability of this program beyond the grant-funded cycle. Specifically, we propose:

  1. To assess racial differences in early-stage breast cancer patients' experiences, beliefs about and barriers to effective adjuvant treatments;
  2. To evaluate the effectiveness of an intervention connecting women with early-stage breast cancer and cancer-related needs to community and hospital-based patient-assistance programs to reduce underuse of effective adjuvant breast cancer treatment overall and in minority populations and to assess its sustainability; and
  3. To evaluate whether this patient assistance intervention affects patients' knowledge, attitudes and behaviors
Being tested
Patient Assistance, Information only
Keywords
breast cancer, adjuvant treatment, racial disparities
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Patient AssistanceBehavioural

    Patients will be surveyed to assess their knowledge about cancer \& its treatment, experience with \& access to health care system, trust, depression, social support \& self-efficacy. A Brief Screening Needs Assessment will be done to ascertain practical, informational or psychosocial needs; based on their responses, an individualized action plan to connect with patient assistance programs will be created for the intervention group. We will ask intervention patients if they connected with any programs in their action plan. For those who didn't connect, we will give their name to an outreach worker. The outreach worker will call patients and identify reasons for not contacting the assistance programs.

  • Information onlyBehavioural

    Control patients will be sent a pamphlet about breast cancer \& its treatment. We will call all patients 2 weeks later and ask if they received the packet. If they didn't, we will send the packet again.

Study groups in NCT00233077
Study groupRoleWhat they receive
Behavioral: Patient AssistanceExperimentalPatient assistance programs
Receives: Behavioral: Patient Assistance
Control: Information onlyOtherControl patients will be sent a pamphlet about breast cancer \& its treatment. We will call all patients 2 weeks later and ask if they received the packet. If they didn't, we will send the packet again.
Receives: Behavioral: Information only

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. initiation and completion of primary treatment

    Measured: Measured after completion of 6-mth interview

Secondary outcomes (5)
  1. adherence

    Measured: Measured after completion of 6-mth interview

  2. emotional and health status

    Measured: Measured at baseline

  3. emotional and health status

    Measured: Measured after completion of 6-mth interview

  4. patient satisfaction

    Measured: measured at baseline

  5. patient satisfaction

    Measured: Measured after completion of 6-mth interview

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Oct 2005 (estimated)
  2. Study startOct 2006
  3. Primary completionJun 2010
  4. Study completionJan 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
374 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00233077
Sponsor's protocol ID
GCO 03-0593
Other IDs
1R01CA10705-01A1
Status last verified
Dec 2013
First submitted
3 Oct 2005
Last updated
3 Dec 2013
Results posted
No
Data monitoring committee
Yes

Publications

  • Guth AA, Fineberg S, Fei K, Franco R, Bickell NA. Utilization of Oncotype DX in an Inner City Population: Race or Place? Int J Breast Cancer. 2013;2013:653805. doi: 10.1155/2013/653805. Epub 2013 Dec 18.

    PubMed 24455283
  • Bickell NA, Geduld AN, Joseph KA, Sparano JA, Kemeny MM, Oluwole S, Menes T, Srinivasan A, Franco R, Fei K, Leventhal H. Do community-based patient assistance programs affect the treatment and well-being of patients with breast cancer? J Oncol Pract. 2014 Jan;10(1):48-54. doi: 10.1200/JOP.2013.000920. Epub 2013 Sep 10.

    PubMed 24023271
  • Lin JJ, Fei K, Franco R, Bickell NA. Breast cancer patients' recall of receiving patient assistance services. Springerplus. 2012 Oct 3;1:24. doi: 10.1186/2193-1801-1-24. eCollection 2012.

    PubMed 23961354

Questions about this trial

What is this clinical trial studying?

A study testing Patient Assistance and Information only in people with Early-Stage Breast Cancer, run by Icahn School of Medicine at Mount Sinai at 8 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Dec 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

initiation and completion of primary treatment (time frame: Measured after completion of 6-mth interview). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00233077, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Dec 2013.

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