- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07475130
Utfordre oddsen: Treningstips og motivasjonsstrategier for stillesittende jobber
Tross oddsen: Treningsprognoser og motivasjonsstrategier for stillesittende jobber
This study aims to see if a new approach called "Exercise Forecasting" can help people with jobs with a lot of sitting get more active. It also tests if using this method in personal motivational messages makes it easier for them to exercise.
The main questions it aims to answer are:
- Can "Exercise Forecasting" be used effectively for people in jobs requiring long periods of sitting?
- Do these tailored, proactive messages encourage people to exercise more and sit less?
Participants will:
- Wear the provided smartwatch and answer two questions per day
- Receive customized motivational messages
Studieoversikt
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
Wisconsin
-
Madison, Wisconsin, Forente stater, 53705
- University of Wisconsin - Madison
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Can communicate in English
- Currently participate in less than 30 minutes of regular physical activity per week.
- Healthy male/female, age >=40
- Currently working in a prolonged sitting job (e.g., truck driver or office worker).
- Have been working in this industry/business for at least one year.
Exclusion Criteria:
- Have had a heart attack within the past three months
- Surgery in the past three months
- Recent stroke, mini-stroke/TIA in the past three months
- Recent seizure disorder or epilepsy in the past three months
- Had an aortic aneurysm before
- Have a medical condition or physical limitation that makes physical activity unsafe
- Currently meeting or exceeding physical activity guidelines (≥150 minutes/week of moderate-intensity activity or equivalent).
- Cannot wear a smartwatch for 30 days.
- Do not want to install a study APP in smart phone for 30 days.
- Cannot respond to the study APP notification for 30 days.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Office workers
Participants who are office workers |
Participants receive motivational messages customized to their previously stated expectations and goals. |
|
Eksperimentell: Truck drivers
Participants who are truck drivers |
Participants receive motivational messages customized to their previously stated expectations and goals. |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Correlation between biometric data and self-reported exercise
Tidsramme: 20 days
|
Biometric data will be collected through the smartwatch. Participants are also asked to self-report what type of exercise they did. These will be correlated to learn whether probability of daily activity can be predicted. |
20 days
|
|
Acceptability of customized messages
Tidsramme: 30 days
|
Acceptability will be qualitatively evaluated using one-on-one interviews, with semi-structured interview guides. Acceptability will be analyzed using thematic analyses. |
30 days
|
|
Feasibility - retention rate
Tidsramme: 30 days
|
Retention rate will be measured by the number of participants who complete the study. |
30 days
|
|
Change in level of physical activity when receiving custom motivational messages
Tidsramme: Baseline to 30 days
|
Using data collected from the smartwatch, level of physical activity will be compared between pre-motivational messaging and post-motivational messaging. |
Baseline to 30 days
|
|
Change in System Usability Scale (SUS) Score
Tidsramme: Baseline to 30 days
|
SUS is a 10-item questionnaire about system usability. It is scored on a 5-point Likert scale, where 1 = strongly disagree and 5 = strongly agree. Scores range from 0-100 (due to reverse scoring and 2.5 multiplication). Higher scores indicate greater usability. |
Baseline to 30 days
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Wan-chin Kuo, PhD, RN, University of Wisconsin, Madison
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- 2026-0224
- UWMSN | Nursing | Administrati (Annen identifikator: UW Madison)
- T42OH008434 (U.S. NIH-stipend/kontrakt)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .