- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03108651
Mobile Motivational Messages for Change (3M4Chan) Intervention in TMU
8. april 2019 opdateret af: 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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
92
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Taipei, Taiwan, 11031
- Syed Abdul Shabbir
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
20 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Case
Motivational message will be administrated.
|
Motivational message will be administrated.
|
|
Ingen indgriben: Control
Motivational message will not be administrated.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Smoking cessation rate at two months
Tidsramme: Up to 2 months
|
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.
|
Up to 2 months
|
|
Smoking cessation rate at four months
Tidsramme: Up to 4 months
|
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.
|
Up to 4 months
|
|
Smoking cessation rate at six months
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
User engagement at an individual level
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
|
Engagement at aggregated level - Mobile application rolling retention
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
|
Engagement at aggregated level - Mobile application session length distribution
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
|
Engagement at aggregated level - Mobile application session frequency
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
|
Engagement at aggregated level - Mobile application sessions per user
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
|
Engagement at aggregated level - Mobile application return rate
Tidsramme: Up to 6 months
|
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.
|
Up to 6 months
|
|
User quitting attempts
Tidsramme: Up to 6 months
|
Number of quitting attempts per patient, including the frequency of the quitting attempts.
|
Up to 6 months
|
|
User app behavior
Tidsramme: Up to 6 months
|
It will be measured as the time spent per app section.
|
Up to 6 months
|
|
User satisfaction with messages
Tidsramme: At 6 months after enrolment.
|
Patients' answers to a satisfaction questionnaire that will be handed to them at the end of the study.
|
At 6 months after enrolment.
|
|
User message ratings
Tidsramme: Up to 6 months
|
User's votes for each message in a 5 star scale.
|
Up to 6 months
|
|
User lifestyle feedback
Tidsramme: At enrollment and at 6 months after enrollment
|
Comparison of changes in user lifestyle (at baseline and after 6 months) through the combined questionnaire EQ-5D-5L.
|
At enrollment and at 6 months after enrollment
|
|
User lifestyle feedback
Tidsramme: At enrollment and at 6 months after enrollment
|
Comparison of changes in user lifestyle (at baseline and after 6 months) through the combined questionnaire IPAQ for physical activity.
|
At enrollment and at 6 months after enrollment
|
|
User lifestyle feedback
Tidsramme: At enrollment and at 6 months after enrollment
|
Comparison of changes in user lifestyle (at baseline and after 6 months) through the combined questionnaires SF-36.
|
At enrollment and at 6 months after enrollment
|
|
Physical activity
Tidsramme: Up to 6 months
|
The physical activity would be measured as the total time (minutes) of activity per user, retrieved by GoogleFit in the app.
|
Up to 6 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. september 2017
Primær færdiggørelse (Faktiske)
2. marts 2019
Studieafslutning (Faktiske)
15. marts 2019
Datoer for studieregistrering
Først indsendt
24. marts 2017
Først indsendt, der opfyldte QC-kriterier
5. april 2017
Først opslået (Faktiske)
11. april 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
10. april 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
8. april 2019
Sidst verificeret
1. april 2019
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- N201702069
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Case
-
University of PittsburghAfsluttetHalspulsåren stenoseForenede Stater
-
Treatment Research InstituteNational Institute on Drug Abuse (NIDA)Afsluttet
-
Soterix MedicalAfsluttet
-
Sichuan Provincial People's HospitalRekruttering
-
The First Affiliated Hospital of University of...Aktiv, ikke rekrutterendeIskæmisk slagtilfælde | Carotis stenose | Carotisarteriesygdomme | Cerebral revaskulariseringKina
-
The First Affiliated Hospital with Nanjing Medical...RekrutteringIskæmisk slagtilfælde | Halspulsårestenose uden infarkt (lidelse)Kina
-
University of OxfordBritish Heart Foundation; NHS Health Technology Assessment Programme; BUPA...Aktiv, ikke rekrutterendeCarotis stenoseDet Forenede Kongerige, Holland, Belgien, Tyskland, Grækenland, Sverige, Kina, Spanien, Norge, Kroatien, Brasilien, Italien, Østrig, Ungarn, Canada, Israel, Polen, Tjekkiet, Schweiz, Irland, Forenede Stater, Bulgarien, Egypten, Estland, ... og mere
-
Xuanwu Hospital, BeijingRekrutteringHalspulsåreplak | Halspulsåren stenting | Carotis endarterektomiKina