跳至主要内容
临床试验/NCT04379570
NCT04379570进行中(未招募)3 期

Optimizing Endocrine Therapy Through Motivational Interviewing and Text Interventions

Alliance for Clinical Trials in Oncology580 个研究点 分布在 1 个国家目标入组 1,167 人开始时间: 2021年2月15日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
1,167
试验地点
580
主要终点
Endocrine therapy (ET) adherence at 12 months post-randomization

研究概览

简要总结

This phase III trial compares an additional support program (text message reminders and/or telephone-based counseling) with usual care in making sure breast cancer patients take their endocrine therapy medication as prescribed (medication adherence). Medication adherence is how well patients take the medication as prescribed by their doctors, and good medical adherence is when patients take medications correctly. Poor medication adherence has been shown to be a serious barrier to effective treatment for hormone receptor positive breast cancer patients. Adding text message reminders and/or telephone-based counseling to usual care may increase the number of days that patients take their endocrine therapy medication as prescribed.

详细描述

PRIMARY OBJECTIVES:

I. Compare endocrine therapy (ET) adherence at 12 months in diverse women exposed to text message reminders (TMR)-only, telephone-based motivational interviewing counseling (MI)-only, or both (TMR+MI), versus usual care.

SECONDARY OBJECTIVES:

l. Compare endocrine therapy (ET) adherence at 24 months in diverse women exposed to text message reminders (TMR)-only, telephone-based motivational interviewing counseling (MI)-only, or both (TMR+MI), versus usual care.

OUTLINE: Patients are randomized to 1 of 4 arms.

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
否

入选标准

  • •Women with an initial pathologically confirmed diagnosis of stage I-III, hormone receptor positive, HER2-neu negative, invasive breast cancer within 18 months prior to enrollment
  • •Women who have undergone neo-adjuvant chemotherapy who have no residual invasive disease post-surgery are eligible based on an initial pathologically confirmed diagnosis
  • •Hormone receptor positive is defined as estrogen receptor (ER) and/or progesterone receptor (PR) of > 1%
  • •HER2-neu negative is defined as 0-1+ by immunohistochemical (IHC) analysis, or non-amplified by fluorescence in situ hybridization (FISH) analysis
  • •Patients must have received cancer-directed surgery, and/or completed all other adjuvant therapy, except reconstruction
  • •Patients must have initiated an endocrine therapy drug within the 6 months prior to registration, OR have received a prescription with stated intent to initiate within 6 weeks after registration
  • •No history of previous cancer as follows:
  • •Invasive or non-invasive breast cancer at any time
  • •Non-breast cancer, within the past 5 years, excluding non-melanoma skin cancer
  • •Patients must be willing to use a smart phone for study activities
  • •Patient is NOT to be deemed ineligible during the recruitment process if they do not have a smart phone
  • •If a participant does not own a smart phone or has limited data or texting capabilities or their smart phone cannot support the Alliance electronic patient reported outcomes (ePRO) survey application (app), a smart phone and service can be provided to the participant at no cost through the Ohio State University (OSU) partnership with Verizon Wireless for the duration of the study activities
  • •The CRP is ONLY to discuss this option with those patients who self-identify a phone-related barrier to participation, including: lack of a smart phone, insufficient phone plan (minutes/text/data), or a smart phone incompatible with the Alliance ePRO app
  • •For OSU -provided phones, charges will be paid by the grant through the intervention period. At the end of the 12-month intervention period, patients will be responsible for paying monthly fees, if continued service is desired. The physical phones will belong to the patients at the end of their study activities
  • •Patients must be willing to use a Pillsy medication event monitoring system for the duration of study participation
  • •In order to complete the mandatory patient-completed measures, participants must be able to speak and read English

排除标准

  • 未提供

研究组 & 干预措施

Arm I (TMR)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive daily text message reminders to take their ET medication and monthly text messages about how they are doing with taking their ET medication. These text messages continue for 9 months.

干预措施: Educational Intervention (Other)

Arm I (TMR)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive daily text message reminders to take their ET medication and monthly text messages about how they are doing with taking their ET medication. These text messages continue for 9 months.

干预措施: Text Message-based Navigation Intervention (Other)

Arm I (TMR)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive daily text message reminders to take their ET medication and monthly text messages about how they are doing with taking their ET medication. These text messages continue for 9 months.

干预措施: Questionnaire Administration (Other)

Arm I (TMR)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive daily text message reminders to take their ET medication and monthly text messages about how they are doing with taking their ET medication. These text messages continue for 9 months.

干预措施: Quality-of-Life Assessment (Other)

Arm II (MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive a total of 5 motivational interviewing counseling sessions via telephone over 30-90 minutes for up to 9 months. These sessions are designed to support patients while they take their ET medication, develop health goals, and stay on track in achieving those goals.

干预措施: Educational Intervention (Other)

Arm II (MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive a total of 5 motivational interviewing counseling sessions via telephone over 30-90 minutes for up to 9 months. These sessions are designed to support patients while they take their ET medication, develop health goals, and stay on track in achieving those goals.

干预措施: Motivational Interviewing (Behavioral)

Arm II (MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive a total of 5 motivational interviewing counseling sessions via telephone over 30-90 minutes for up to 9 months. These sessions are designed to support patients while they take their ET medication, develop health goals, and stay on track in achieving those goals.

干预措施: Questionnaire Administration (Other)

Arm II (MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive a total of 5 motivational interviewing counseling sessions via telephone over 30-90 minutes for up to 9 months. These sessions are designed to support patients while they take their ET medication, develop health goals, and stay on track in achieving those goals.

干预措施: Quality-of-Life Assessment (Other)

Arm III (TMR + MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive text messages as in Arm I and motivational interviewing counseling sessions as in Arm II.

干预措施: Educational Intervention (Other)

Arm III (TMR + MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive text messages as in Arm I and motivational interviewing counseling sessions as in Arm II.

干预措施: Text Message-based Navigation Intervention (Other)

Arm III (TMR + MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive text messages as in Arm I and motivational interviewing counseling sessions as in Arm II.

干预措施: Motivational Interviewing (Behavioral)

Arm III (TMR + MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive text messages as in Arm I and motivational interviewing counseling sessions as in Arm II.

干预措施: Questionnaire Administration (Other)

Arm III (TMR + MI)

Experimental

Patients receive online educational information about ET at the start of their ET medication. Patients also receive text messages as in Arm I and motivational interviewing counseling sessions as in Arm II.

干预措施: Quality-of-Life Assessment (Other)

Arm IV (enhanced usual care)

Active Comparator

Patients attend usual care clinic visits every 3-6 months and receive online educational information about ET at the start of their ET medication. Patients also receive optional online information about living a healthy life after breast cancer.

干预措施: Educational Intervention (Other)

Arm IV (enhanced usual care)

Active Comparator

Patients attend usual care clinic visits every 3-6 months and receive online educational information about ET at the start of their ET medication. Patients also receive optional online information about living a healthy life after breast cancer.

干预措施: Best Practice (Other)

Arm IV (enhanced usual care)

Active Comparator

Patients attend usual care clinic visits every 3-6 months and receive online educational information about ET at the start of their ET medication. Patients also receive optional online information about living a healthy life after breast cancer.

干预措施: Questionnaire Administration (Other)

Arm IV (enhanced usual care)

Active Comparator

Patients attend usual care clinic visits every 3-6 months and receive online educational information about ET at the start of their ET medication. Patients also receive optional online information about living a healthy life after breast cancer.

干预措施: Quality-of-Life Assessment (Other)

结局指标

主要结局

Endocrine therapy (ET) adherence at 12 months post-randomization

时间窗: At 12 months post-randomization

ET adherence at 12 months post-randomization will be measured by electronic pill monitoring cap (Pillsy-reported) and defined as the proportion of patients within each arm who have taken their ET medication for at least 292 of 365 days.

次要结局

  • Endocrine therapy (ET) adherence at 24 months post-randomization(At 24 months post-randomization)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (580)

Loading locations...

相似试验

已完成
2 期
Efficacy Trial of Warrior Check-UpAlcohol DependenceAlcohol AbuseSubstance AbuseSubstance Dependence
NCT01128140University of Washington242
进行中(未招募)
不适用
A Text-based Intervention in Improving Adherence to Hormone Therapy in Patients With Stage I-III Hormone Receptor Positive Breast CancerAnatomic Stage IIIB Breast Cancer AJCC v8Estrogen Receptor Positive TumorPrognostic Stage IIIA Breast Cancer AJCC v8Anatomic Stage I Breast Cancer AJCC v8Progesterone Receptor Positive TumorAnatomic Stage III Breast Cancer AJCC v8Anatomic Stage IIIA Breast Cancer AJCC v8Anatomic Stage IIB Breast Cancer AJCC v8Anatomic Stage IIIC Breast Cancer AJCC v8Anatomic Stage IIA Breast Cancer AJCC v8Anatomic Stage IA Breast Cancer AJCC v8Anatomic Stage II Breast Cancer AJCC v8Prognostic Stage IIA Breast Cancer AJCC v8Prognostic Stage IIB Breast Cancer AJCC v8Prognostic Stage III Breast Cancer AJCC v8Prognostic Stage IIIC Breast Cancer AJCC v8Prognostic Stage IA Breast Cancer AJCC v8Prognostic Stage IB Breast Cancer AJCC v8Prognostic Stage II Breast Cancer AJCC v8Prognostic Stage I Breast Cancer AJCC v8Prognostic Stage IIIB Breast Cancer AJCC v8
NCT04086875Thomas Jefferson University332
已完成
不适用
Patient Reported Outcomes, Smart Pill Bottle and Teleheath for Endocrine Therapy AdherenceStage 0 Breast Cancer AJCC v6 and v7Stage I Breast Cancer AJCC v7Stage IB Breast Cancer AJCC v7Stage II Breast Cancer AJCC v6 and v7Stage IIA Breast Cancer AJCC v6 and v7Stage IIIA Breast Cancer AJCC v7Stage IIIB Breast Cancer AJCC v7Stage IIIC Breast Cancer AJCC v7Stage III Breast Cancer AJCC v7Stage IA Breast Cancer AJCC v7Stage IIB Breast Cancer AJCC v6 and v7
NCT04054557Thomas Jefferson University305
已完成
不适用
Telephone-Based Intervention in Increasing Adherence to Adjuvant Hormonal Therapy in Patients With Breast CancerStage IIIA Breast CancerStage IIIB Breast CancerStage IA Breast CancerStage IB Breast CancerStage IIIC Breast CancerStage IIB Breast CancerStage 0 Breast CancerStage IIA Breast Cancer
NCT02400060Ohio State University Comprehensive Cancer Center39
已完成
不适用
Text Messaging for Supporting Quit AttemptsTobacco Use CessationTobacco Use Disorder
NCT02571244Federal University of Juiz de Fora66
Additional Support Program Via Text Messaging and... | 临床试验