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临床试验/NCT03346161
NCT03346161已完成1 期

Optimizing Decision Making About Breast Reconstruction After Mastectomy: A Patient-Centered Approach

Washington University School of Medicine2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2018年1月9日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
120
试验地点
2
主要终点
Decision Process (Decision Quality Index Subscale)

研究概览

简要总结

Although clinical decision tools (CDTs) exist for a variety of treatments, CDTs designed to support personalized breast reconstruction decisions, particularly about type and timing of reconstruction, are lacking. The objective of this proposal is to develop and pilot test a clinical decision tool that provides personalized risk information and reflects patients' preferences and clinical needs.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Arm 1: BREASTChoice (Decision Tool)

Experimental

Investigators recruited patients scheduled for a plastic/reconstruction consult. Investigators identified patients who completed a mastectomy, or were scheduled for one, and considering reconstruction, but didn't have an appointment with a plastic/reconstructive surgeon. A study team member called the patient to determine their interest and offered for them to come to their scheduled appointment 30 minutes early to meet a coordinator or offered them the option to complete pre-appointment procedures at home. Patients randomized using computer random assignment. If the patient didn't have an appointment, she scheduled a convenient time to complete study procedures with research staff. Patients interacted with the decision tool. They were asked to answer a survey. After the appointment, the team collected information consult duration, decision process quality, and measures of shared decision making. Patient participation was approximately 30 minutes.

干预措施: Decision tool (Other)

Arm 1: BREASTChoice (Decision Tool)

Experimental

Investigators recruited patients scheduled for a plastic/reconstruction consult. Investigators identified patients who completed a mastectomy, or were scheduled for one, and considering reconstruction, but didn't have an appointment with a plastic/reconstructive surgeon. A study team member called the patient to determine their interest and offered for them to come to their scheduled appointment 30 minutes early to meet a coordinator or offered them the option to complete pre-appointment procedures at home. Patients randomized using computer random assignment. If the patient didn't have an appointment, she scheduled a convenient time to complete study procedures with research staff. Patients interacted with the decision tool. They were asked to answer a survey. After the appointment, the team collected information consult duration, decision process quality, and measures of shared decision making. Patient participation was approximately 30 minutes.

干预措施: Decision Group - Outcome Measures (Other)

Arm 1: BREASTChoice (Decision Tool)

Experimental

Investigators recruited patients scheduled for a plastic/reconstruction consult. Investigators identified patients who completed a mastectomy, or were scheduled for one, and considering reconstruction, but didn't have an appointment with a plastic/reconstructive surgeon. A study team member called the patient to determine their interest and offered for them to come to their scheduled appointment 30 minutes early to meet a coordinator or offered them the option to complete pre-appointment procedures at home. Patients randomized using computer random assignment. If the patient didn't have an appointment, she scheduled a convenient time to complete study procedures with research staff. Patients interacted with the decision tool. They were asked to answer a survey. After the appointment, the team collected information consult duration, decision process quality, and measures of shared decision making. Patient participation was approximately 30 minutes.

干预措施: Demographic and Background Questions (Other)

Arm 2: Enhanced Usual Care (Surgical Care Booklet)

Active Comparator

Investigators recruited patients scheduled for plastic/reconstruction consultation. Investigators identified patients who completed or scheduled a mastectomy, and considering reconstruction, but didn't have an appointment with a plastic/reconstructive surgeon. A study team member called the patient to determine their interest and offered for them to come to their scheduled appointment 30 minutes early to meet a coordinator or to complete the pre-appointment procedures at home. Patients were randomized using computer random assignment. If the patient didn't have an appointment, she scheduled a convenient time to complete study procedures with research staff. Patients interacted with American Society of Plastic Surgeons booklet "Breast Reconstruction." They were asked to answer a survey. After the appointment, the team collected information about consult duration, decision process quality, and measures of shared decision making. Patient participation was approximately 30 minutes.

干预措施: Usual care American Society of Plastic Surgeons booklet "Breast Reconstruction" (Other)

Arm 2: Enhanced Usual Care (Surgical Care Booklet)

Active Comparator

Investigators recruited patients scheduled for plastic/reconstruction consultation. Investigators identified patients who completed or scheduled a mastectomy, and considering reconstruction, but didn't have an appointment with a plastic/reconstructive surgeon. A study team member called the patient to determine their interest and offered for them to come to their scheduled appointment 30 minutes early to meet a coordinator or to complete the pre-appointment procedures at home. Patients were randomized using computer random assignment. If the patient didn't have an appointment, she scheduled a convenient time to complete study procedures with research staff. Patients interacted with American Society of Plastic Surgeons booklet "Breast Reconstruction." They were asked to answer a survey. After the appointment, the team collected information about consult duration, decision process quality, and measures of shared decision making. Patient participation was approximately 30 minutes.

干预措施: Usual Care Group - Outcome Measures (Other)

Arm 2: Enhanced Usual Care (Surgical Care Booklet)

Active Comparator

Investigators recruited patients scheduled for plastic/reconstruction consultation. Investigators identified patients who completed or scheduled a mastectomy, and considering reconstruction, but didn't have an appointment with a plastic/reconstructive surgeon. A study team member called the patient to determine their interest and offered for them to come to their scheduled appointment 30 minutes early to meet a coordinator or to complete the pre-appointment procedures at home. Patients were randomized using computer random assignment. If the patient didn't have an appointment, she scheduled a convenient time to complete study procedures with research staff. Patients interacted with American Society of Plastic Surgeons booklet "Breast Reconstruction." They were asked to answer a survey. After the appointment, the team collected information about consult duration, decision process quality, and measures of shared decision making. Patient participation was approximately 30 minutes.

干预措施: Demographic and Background Questions (Other)

结局指标

主要结局

Decision Process (Decision Quality Index Subscale)

时间窗: Through completion of breast consultation appointment (total participant time approximately 30 minutes)

* The total points are summed and then divided by the total number of items to result in scores from 0-100%, with higher scores indicating a more shared decision making process * Assess the extent to which patients were meaningfully involved in decision-making with their clinicians

Percent Correct on the Knowledge Measure (Objective Knowledge Score)

时间窗: Through completion of breast consultation appointment (total participant time approximately 30 minutes)

To determine whether the CDT increases knowledge about their choice, the investigators will compare objective knowledge scores between participants using the CDT and those who received usual care

Decisional Conflict (SURE Measure)

时间窗: Through completion of breast consultation appointment (total participant time approximately 30 minutes)

* To determine whether the CDT reduces uncertainty about choice. Participants are asked to report how sure they feel about their choice, if they have enough information to understand the choice, if they are clear about the risks and benefits, and if they have enough support to make a choice. Results are compared between the BREASTChoice and Enhanced Usual Care groups. * Higher SURE values indicate certainty in choice * Scores range from 0-4

次要结局

  • Quality of Life as Measured by the BREAST-Q Questionnaire(Through completion of breast consultation appointment (total participant time approximately 30 minutes))
  • Patient Activation (PAM) as Measured by the Number of Participants Who Agreed With Each Statement(Through completion of breast consultation appointment (total participant time approximately 30 minutes))
  • Receipt of Reconstruction(Through follow-up (approximately 6 months))
  • Timing of Reconstruction(Through completion of follow-up (approximately 6 months))
  • Consult Time(Through completion of breast consultation appointment (total participant time approximately 30 minutes))
  • Usability as Measured by the Computer System Usability Questionnaire (CSUQ)(Through completion of breast consultation appointment (total participant time approximately 30 minutes))
  • Gold Standard Shared Decision Making as Measured by the Top collaboRATE Score(Through completion of breast consultation appointment (total participant time approximately 30 minutes))
  • Type of Reconstruction(Through completion of follow-up (approximately 6 months))
  • Time Spent on Tool(Through completion of breast consultation appointment (total participant time approximately 30 minutes))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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