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Clinical Trials/NCT05049746
NCT05049746
Active, not recruiting
Not Applicable

Identifying Decision Making Needs for Older Adult Women With Breast Cancer Considering Neoadjuvant or Adjuvant Chemotherapy

M.D. Anderson Cancer Center2 sites in 1 country95 target enrollmentFebruary 23, 2016

Overview

Phase
Not Applicable
Intervention
Discussion
Conditions
Not specified
Sponsor
M.D. Anderson Cancer Center
Enrollment
95
Locations
2
Primary Endpoint
Decision making needs assessment questionnaire
Status
Active, not recruiting
Last Updated
yesterday

Overview

Brief Summary

This study collects information and identifies decision making needs for older adult women with stage I-III breast cancer considering neoadjuvant and adjuvant chemotherapy. Using this information, a decision support tool is then developed to provide patients and physicians with tailored information regarding the risks and benefits of chemotherapy and values clarification to support high-quality, shared decision. Subsequently, the decision support tool will be tested amongst older patients with early-stage breast cancer and health care providers navigating the decision process around chemotherapy, and further refined through an iterative process.

Detailed Description

PRIMARY OBJECTIVES: I. To characterize and describe the informational needs and preferences in older adult women who intend on receiving neoadjuvant or adjuvant chemotherapy for stage I-III breast cancer. Ia. Conduct semi-structured interviews with women who have completed the treatment decision process to collect informational needs and elicit decision-making needs and preferences. Ib. Utilize validated data collection instruments to assess the shared decision-making process and health literacy needs. II. To develop a decision support tool for use by patients and healthcare providers to guide the chemotherapy decision-making process in older women (\>= 65) with early-stage breast cancer. IIa. To conduct cognitive testing of the decision tool. IIb. To conduct a field test of the decision tool in order to demonstrate feasibility and acceptability in real-world clinical settings. OUTLINE: Patients undergo interviews and complete questionnaires over 1-2 hours. Patients and physicians also participate in a discussion and complete shared decision-making questionnaire over 15-30 minutes. Subsequently, a decision support tool will be developed consistent with standards for content development and evaluation from the International Patient Decision Aid Standards (IPDAS) Collaboration and implemented through an iterative process of design, development and evaluation to engage end users in its development. Once developed, field testing of the decision tool will be conducted to demonstrate feasibility and acceptability in real-world clinical setting, followed by pilot testing to evaluate the efficacy of the decision support tool.

Registry
clinicaltrials.gov
Start Date
February 23, 2016
End Date
February 2, 2027
Last Updated
yesterday
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient Inclusion Criteria
  • Women aged 65 years or older
  • Must write and speak English
  • Must have been diagnosed with Stage I-III breast cancer
  • Must have made decision to either receive or not receive neoadjuvant or adjuvant chemotherapy
  • Must be within 3 months of breast cancer neoadjuvant or adjuvant chemotherapy treatment decision
  • Self-reported no visual or auditory deficits
  • SUBAIM 2b: Women aged 65 years or older
  • SUBAIM 2b: Must write and speak English
  • SUBAIM 2b: Must have been diagnosed with stage I-III breast cancer

Exclusion Criteria

  • Not provided

Arms & Interventions

Intervention Arm

Participants in the intervention arm only will then be asked to look at the decision tool that includes educational materials about the diagnosis and treatment of breast cancer. These could be written information, graphics, videos, animations, or questionnaires. This decision tool will personalize the decision to you specifically and support your decision-making process

Intervention: Discussion

Non-Intervention Arm

Participants undergo interviews and complete questionnaires over 1-2 hours. Patients and physicians also participate in a discussion and complete shared decision-making questionnaire over 15-30 minutes.

Intervention Arm

Participants in the intervention arm only will then be asked to look at the decision tool that includes educational materials about the diagnosis and treatment of breast cancer. These could be written information, graphics, videos, animations, or questionnaires. This decision tool will personalize the decision to you specifically and support your decision-making process

Intervention: Interview

Intervention Arm

Participants in the intervention arm only will then be asked to look at the decision tool that includes educational materials about the diagnosis and treatment of breast cancer. These could be written information, graphics, videos, animations, or questionnaires. This decision tool will personalize the decision to you specifically and support your decision-making process

Intervention: Questionnaire Administration

Outcomes

Primary Outcomes

Decision making needs assessment questionnaire

Time Frame: through study completion, an average of 1 year

The mean score of the shared decision making questionnaire and its standard deviation along with the median and the range will be computed for both the patient and physician study population. Score Range-(0-4) 0-Not at all confident 4-very confident

Study Sites (2)

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