Mobile Motivational Messages for Change (3M4Chan) Intervention in TMU
2019년 4월 8일 업데이트: Shabbir Syed Abdul, Taipei Medical University
About 100 (50 from TMU Hospital and 50 from Wellcome Clinic) current smokers will be recruited who contact smoke cession clinics in teaching hospitals of Taipei Medical University (TMU) and Wellcome Clinic.
They will be randomly assigned either to Usual Care (UC) or Usual Care plus 3M4Chan Intervention group (IG).
A randomized comparative effectiveness trial will be conducted.
Patient will enroll from September 2017 to May 2018.
In UC group, the physician provides a brief advice to quit during first consultation, a quit plan template, and medication prescription (Varenicline, Bupropion, Champix, Nicotinell TTS20) as decided by the physician.
IG group includes UC plus a mobile App that is programmed to push tailored messages for health concern and readiness to quit, tips for sustaining abstinence, use of interactive self-assessments, helpful cessation information.
This group of smokers will benefit from tailored cessation interventions with integrated body weight management elements that take into consideration the prevailing local and cultural influences on diet and levels of physical activity.
IG will be continued even after stopping of the UC.
연구 개요
연구 유형
중재적
등록 (실제)
92
단계
- 해당 없음
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Taipei, 대만, 11031
- Syed Abdul Shabbir
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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
20년 이상 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
예
연구 대상 성별
모두
설명
Inclusion Criteria:
- Age 20 years or older and approach smoke cessation clinic at TMU hospital
- Have an Android mobile phone
- Able to read Traditional Chinese
- Willing to participate in all study components
- Willing to be followed-up for 6 months
- Smoked at least once every month in the last two years
- Current smoker
Exclusion Criteria:
• Below 20 years on the day of enrolment
- Not willing to participate in the study
- Those who do not have Android mobile phone or unable to read Mandarin
- Not willing to share medical information from EHR
- Subjects who develop adverse effects related to the pharmacological treatment included in the study
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: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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활성 비교기: Case
Motivational message will be administrated.
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Motivational message will be administrated.
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간섭 없음: Control
Motivational message will not be administrated.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Smoking cessation rate at two months
기간: Up to 2 months
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Smoking cessation rate will be measured as the ratio of the total number of patients who relapsed with total number of patients in their group.
Patients will be considered to have relapsed if they fail at least one of their urine cotinine and carbon monoxide tests.
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Up to 2 months
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Smoking cessation rate at four months
기간: Up to 4 months
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Smoking cessation rate will be measured as the ratio of the total number of patients who relapsed with total number of patients in their group.
Patients will be considered to have relapsed if they fail at least one of their urine cotinine and carbon monoxide tests.
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Up to 4 months
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Smoking cessation rate at six months
기간: Up to 6 months
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Smoking cessation rate will be measured as the ratio of the total number of patients who relapsed with total number of patients in their group.
Patients will be considered to have relapsed if they fail at least one of their urine cotinine and carbon monoxide tests.
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Up to 6 months
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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User engagement at an individual level
기간: Up to 6 months
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Engagement at individual level will be assessed based on the rate of read messages by the patients.
This is calculated as the quotient between the messages the patients have read, and the total number of messages the system has sent to the patients.
This metric will be assessed throughout the observation until its end.
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Up to 6 months
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Engagement at aggregated level - Mobile application rolling retention
기간: Up to 6 months
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The percentage of users still active N days after installation.
This is a ratio of the number of users whose last day of activity is past day N to the number of users who could have been active on day N.
This metric will be assessed throughout the observation until its end.
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Up to 6 months
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Engagement at aggregated level - Mobile application session length distribution
기간: Up to 6 months
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The session length is defined as the length of time between the start of the application event and the end of the application event.
The session length determines the engagement as it is relevant to know how much time patients spend in the app per session.
This metric will be assessed throughout the observation until its end.
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Up to 6 months
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Engagement at aggregated level - Mobile application session frequency
기간: Up to 6 months
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The session frequency is a measure of how often each unique patient used the app within a given time interval.
This metric will be assessed throughout the observation until its end.
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Up to 6 months
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Engagement at aggregated level - Mobile application sessions per user
기간: Up to 6 months
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A session is one use of the mobile application by a patient.
This begins when the application is launched and ends when the application is terminated.
This metric will be assessed throughout the observation until its end.
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Up to 6 months
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Engagement at aggregated level - Mobile application return rate
기간: Up to 6 months
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Return rate measures the percentage of patients who return to the app on a specific time after installation.
It is measured by cohort group - that is, based on when patients first opened the app.
It is calculated as the ratio of the number of users active on a given period to the size of the cohort.
This metric will be assessed throughout the observation until its end.
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Up to 6 months
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User quitting attempts
기간: Up to 6 months
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Number of quitting attempts per patient, including the frequency of the quitting attempts.
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Up to 6 months
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User app behavior
기간: Up to 6 months
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It will be measured as the time spent per app section.
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Up to 6 months
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User satisfaction with messages
기간: At 6 months after enrolment.
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Patients' answers to a satisfaction questionnaire that will be handed to them at the end of the study.
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At 6 months after enrolment.
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User message ratings
기간: Up to 6 months
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User's votes for each message in a 5 star scale.
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Up to 6 months
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User lifestyle feedback
기간: At enrollment and at 6 months after enrollment
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Comparison of changes in user lifestyle (at baseline and after 6 months) through the combined questionnaire EQ-5D-5L.
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At enrollment and at 6 months after enrollment
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User lifestyle feedback
기간: At enrollment and at 6 months after enrollment
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Comparison of changes in user lifestyle (at baseline and after 6 months) through the combined questionnaire IPAQ for physical activity.
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At enrollment and at 6 months after enrollment
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User lifestyle feedback
기간: At enrollment and at 6 months after enrollment
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Comparison of changes in user lifestyle (at baseline and after 6 months) through the combined questionnaires SF-36.
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At enrollment and at 6 months after enrollment
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Physical activity
기간: Up to 6 months
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The physical activity would be measured as the total time (minutes) of activity per user, retrieved by GoogleFit in the app.
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Up to 6 months
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
간행물 및 유용한 링크
연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 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 (실제)
2017년 9월 1일
기본 완료 (실제)
2019년 3월 2일
연구 완료 (실제)
2019년 3월 15일
연구 등록 날짜
최초 제출
2017년 3월 24일
QC 기준을 충족하는 최초 제출
2017년 4월 5일
처음 게시됨 (실제)
2017년 4월 11일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2019년 4월 10일
QC 기준을 충족하는 마지막 업데이트 제출
2019년 4월 8일
마지막으로 확인됨
2019년 4월 1일
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- N201702069
약물 및 장치 정보, 연구 문서
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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. .
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