이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

공동 연구 : 장기 약물 개선을위한 멀티 스케일 모델링 및 개입

2026년 10월 1일 업데이트: San Diego State University

사람들이 장기 의약품을 준수 할 수 있도록 기술 기반 시스템을 배포하고 평가합니다.

The goal of this study is to learn about the impact of an integrated medication monitoring system in breast cancer survivors aged 21-70 who are prescribed endocrine therapy. The main question it aims to address is: Does the integrated medication monitoring system improve medication adherence among breast cancer survivors when used over a six-month period?

Fifteen English-speaking breast cancer survivors who meet the inclusion criteria will use a combination of smartphone-based ecological momentary assessments, a medication event monitoring system (Wisepill), and a wearable sensor (Fitbit). After 2 months, participants will be provided personalized content to facilitate medication adherence through an app (Digital Trails) and through WisePill. Participants will complete online surveys at baseline, 3 months, and 6 months to assess their experiences and adherence.

연구 개요

상세 설명

Purpose/objective:

The investigators have created a new integrated medication monitoring (MM) system for long-term monitoring of medication adherence consisting of baseline, 3-month, and 6-month surveys, smartphone based ecological momentary assessment, smartphone sensors, a medication event monitoring system (MEMS; Wisepill) sensor, and a wrist-worn wearable sensor (Fitbit) that will be used to collect data to understand and model medication-taking behaviors. The objective of the project is to deploy this system to predict nonadherence to endocrine therapy for breast cancer survivors and implement intervention strategies to improve medication adherence. These interventions will be evaluated for preliminary impact on behavior, acceptability, attractiveness, and usefulness.

Overview:

The investigators will conduct a single arm study collecting data in multiple ways and multiple intervals, over six months' time: 1) baseline, 3-month, and 6-month surveys via Qualtrics; 2) smartphone-based ecological momentary assessment (via Digital Trails application) at the following intervals: every 2-3 days, weekly, and monthly; 3) wireless medication event monitoring system devices (MEMS; Wisepill; daily), 4) a wrist-worn wearable sensor (Fitbit; continuous); and 5) smartphone sensors (data collected via Digital Trails application, continuous). Participants will be provided personalized intervention content based on their specific risk via the Digital Trials app. Fifteen breast cancer survivors will be asked to participate in this longitudinal study for six months.

Intervention:

The investigators have created a new integrated medication monitoring (MM) system consisting of baseline, 3-month, and 6-month surveys, smartphone-based ecological momentary assessment via an application installed on a smartphone (Digital Trails based on the UVA Sensus app), a wireless medication event monitoring system device (MEMS; Wisepill), and a wearable sensor (Fitbit), and data collected passively from smartphone sensors using the Digital Trails app. These sources of information will be used to understand predictors of medication taking behaviors and, after two months of monitoring, to deploy appropriate interventions which will be delivered via the Digital Trails app platform. The objective of the project is to deploy this MM system to predict nonadherence to endocrine therapy for breast cancer survivors and implement intervention strategies to improve medication adherence (via Digital Trails). These interventions will be evaluated for preliminary impact on behavior, acceptability, attractiveness, and usefulness.

Participant Eligibility Criteria Fifteen breast cancer survivors will be included in the study if they: 1) are English-speaking and reading; 2) are between ages 21 and 70 years; 3) are diagnosed with stage 0-3 breast cancer in the past 5 years; 4) have completed all surgery, radiation, and chemotherapy, except endocrine therapy; 5) are prescribed endocrine therapy; 6) do not have a physical impairment that would prevent them from using the MM system; 7) are able to provide informed consent; 8) are willing and able to use the MM system for 6 months; and 9) have an Iphone or Android phone.

Participant Recruitment Using convenience sampling, the investigators will recruit 15 breast cancer survivors. The study will be publicized using a number of different ways, including ads on social media. Participants will be directed to complete an online screening survey via Qualtrics or to contact the study staff via email or phone. The investigators will contact interested participants and do a telephone or HIPAA-Zoom screening to assess study inclusion criteria, after obtaining informed consent. The investigators will then provide sensors to participants (via mail) and in a subsequent baseline data collection session (via Zoom), assist participants with completing baseline surveys via Qualtrics, in learning how to use the sensors, and in downloading and using smartphone applications. Participants will be asked to use two sensors: 1) a medication event monitoring system device (MEMS; Wisepill); and 2) a wrist-worn wearable sensor (Fitbit) daily for the next 6 months (see below). Participants will be asked to download the Fitbit and Digital Trails apps to their smartphones. Participants will also be asked to complete ecological momentary assessment (EMA; short surveys) using a smartphone app (Digital Trails) for six months.

Data Collection Digital Trails is an app that combines Sensus, a novel mobile sensing system for Android and iOS capable of collecting data from smartphone and Bluetooth-enabled sensors and administering EMAs, with a smartphone intervention. EMA surveys will be implemented at the following intervals: 1) randomly; 2) every 2- 3 days; 3) every 14 days; and 4) every 28 days. Digital Trails will also collect data from the participants' smartphone if authorized by the participant. These may include, but are not limited to, GPS, accelerometer, gyroscope, and pedometer data. Participants will complete 3 surveys via Qualtrics, at baseline, three month follow-up, and six-month follow-up. These surveys will be administered via Qualtrics. Participants will be asked to use two sensors daily for the entire six month period: 1) a Fitbit wrist sensor; and 2) a Wisepill MEMS cap. The investigators will use the Fitbit Sense smartwatch to collect data including steps, calories burned, total distance traveled, sleep, flights of stairs climbed, active minutes, exercise, and average heart rate. Participants will be asked to download the Fitbit app onto their personal smartphone. Participants' Fitabase data will be monitored by the study team using the Fitabase dashboard.

Primary Outcomes: Adherence to medication, receipt of intervention components, perception of intervention (thoughts, most useful components, lease useful components, most attractive components, least attractive components, problems with the intervention, suggested changes to intervention, additional information that should be provided by intervention, willingness to use intervention/system in future).

Planned analyses:

Evaluation of immediate response to delivery of each intervention module will consist of examining MM data that measure: 1) detection of a risk for missed medication; 2) delivery of the specific intervention module suggested by our modeling; and 3) whether the participant subsequently took the medicine as prescribed after the intervention module was deployed (within a 24 hour interval from the last dose plus or minus 6 hours). The investigators will also summarize data regarding participants' use of each type of module offered and their assessment of the acceptability, attractiveness, and usefulness of intervention modules used. Data collected from close-ended questions (i.e., use of an intervention module) will be summarized using descriptive data (i.e., counts and frequencies). Qualitative data collected from open-ended questions will be summarized using content analysis by having two raters code data on the three a priori themes (i.e., acceptability, attractiveness, and usefulness).

연구 유형

중재적

등록 (추정된)

15

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Kristen J Wells, PhD
  • 전화번호: 619-594-1919
  • 이메일: kwells@sdsu.edu

연구 연락처 백업

연구 장소

    • California
      • San Diego, California, 미국, 92120
        • San Diego State University
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

21년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

여성

설명

Inclusion Criteria:

  • are English-speaking and reading;
  • are between ages 21 and 70 years;
  • are diagnosed with stage 0-3 breast cancer in the past 5 years;
  • have completed all surgery, radiation, and chemotherapy, except endocrine therapy;
  • are prescribed endocrine therapy;
  • do not have a physical impairment that would prevent them from using the MM system;
  • are able to provide informed consent;
  • are willing and able to use the MM system for 6 months;
  • have an Iphone or Android phone.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 지지 요법
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: integrated medication monitoring system

The single-arm intervention design of this study focuses on delivering a comprehensive integrated medication monitoring system to a cohort of breast cancer survivors. The system will analyze data collected from EMAs, MEMS, and Fitbit sensors to identify participants at risk of nonadherence. Based on this risk assessment, personalized interventions will be delivered through the Digital Trails app, which may include reminders for medication intake, among others.

We have created a new integrated medication monitoring (MM) system consisting of baseline, 3-month, and 6-month surveys, smartphone-based ecological momentary assessment via an application installed on a smartphone (Digital Trails based on the UVA Sensus app), a wireless medication event monitoring system device (MEMS; Wisepill), and a wearable sensor (Fitbit), and data collected passively from smartphone sensors using the Digital Trails app. These sources of information will be used to understand predictors of medication taking behaviors and, after two months of monitoring, to deploy appropriate interventions which will be delivered via the Digital Trails app platform.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Wisepill MEMS Sensor data collection
기간: From enrollment to the end of study at 6 months

Participants will be asked to put their endocrine therapy medication in the Wisepill device and will be asked to open the Wisepill when taking their medicine daily for six months

From enrollment to the end of study at 6 months
Intervention component - Introduction
기간: 6 months after enrollment into study

Number of respondents who reported receiving and/or using the app introduction

6 months after enrollment into study
Intervention component - Instructions
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using instructions for using the app

6 months after enrollment into the study
Intervention component - calendar
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using the app calendar

6 months after enrollment into the study
Intervention component - resources
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using resources for breast cancer survivors

6 months after enrollment into the study
Intervention component - relaxation audio files
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using relaxation audio files

6 months after enrollment into the study
Intervention component - social support
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about social support

6 months after enrollment into the study
Intervention component - tamoxifen
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about tamoxifen

6 months after enrollment into the study
Intervention component - aromatase inhibitors
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about aromatase inhibitors

6 months after enrollment into the study
Intervention component - routine
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about establishing a routine for taking medications

6 months after enrollment into the study
Intervention component - reminders
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about setting medication reminders

6 months after enrollment into the study
Intervention component - joint pain
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about managing joint pain

6 months after enrollment into the study
Intervention component - hot flashes
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about managing hot flashes

6 months after enrollment into the study
Intervention component - pacing
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about pacing

6 months after enrollment into the study
Intervention component - relaxation
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about relaxation

6 months after enrollment into the study
Intervention component - needs
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about getting what they need from their health care providers

6 months after enrollment into the study
Intervention component - travel
기간: 6 months after enrollment into the study

Number of respondents who reported receiving and/or using information about travel

6 months after enrollment into the study
Intervention component - thoughts
기간: 6 months after enrollment into the study

Participants will be asked to describe what they thought about the intervention overall (qualitative response)

6 months after enrollment into the study
Intervention component - most useful
기간: 6 months after enrollment into the study

Participants will be asked to describe the most useful intervention components (qualitative response)

6 months after enrollment into the study
Intervention component - least useful
기간: 6 months after enrollment into the study

Participants will be asked to describe the least useful intervention components (qualitative response)

6 months after enrollment into the study
Intervention component - most attractive
기간: 6 months after enrollment into the study

Participants will be asked to describe which intervention components were most attractive (qualitative response)

6 months after enrollment into the study
Intervention component - least attractive
기간: 6 months after enrollment into the study

Participants will be asked to describe which intervention components were least attractive (qualitative response)

6 months after enrollment into the study
Intervention component - problems
기간: 6 months after enrollment into the study

Participants will be asked to describe problems they experienced using the intervention application (qualitative response)

6 months after enrollment into the study
Intervention component - changes
기간: 6 months after enrollment into the study

Participants will be asked to describe any changes they would make to the intervention (qualitative response)

6 months after enrollment into the study
Intervention component - additional information
기간: 6 months after enrollment into the study

Participants will be asked to describe what additional information the intervention should provide (qualitative response)

6 months after enrollment into the study
Intervention component - future use
기간: 6 months after enrollment into the study

Participants will be asked to describe whether or not they would be willing to use the intervention and monitoring system in the future to remember to take medicines.

6 months after enrollment into the study

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 12월 1일

기본 완료 (추정된)

2026년 12월 1일

연구 완료 (추정된)

2026년 12월 1일

연구 등록 날짜

최초 제출

2024년 10월 15일

QC 기준을 충족하는 최초 제출

2025년 3월 3일

처음 게시됨 (실제)

2025년 3월 10일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 1일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

IPD 계획 설명

We plan to share the data so it can be anonymized in registries such as Open Science Framework or alongside our publications.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다