- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07475130
Trotsa Oddsen: Träningsprognoser och Motiveringsstrategier för Långvarigt Sittande Jobb
Trotsa Oddsen: Träningsprognoser och Motivationsstrategier för Långvarigt Stillasittande Jobb
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
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Wisconsin
-
Madison, Wisconsin, Förenta staterna, 53705
- University of Wisconsin - Madison
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
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
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Office workers
Participants who are office workers |
Participants receive motivational messages customized to their previously stated expectations and goals. |
|
Experimentell: Truck drivers
Participants who are truck drivers |
Participants receive motivational messages customized to their previously stated expectations and goals. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Correlation between biometric data and self-reported exercise
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
|
Samarbetspartners och utredare
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Wan-chin Kuo, PhD, RN, University of Wisconsin, Madison
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- 2026-0224
- UWMSN | Nursing | Administrati (Annan identifierare: UW Madison)
- T42OH008434 (U.S.S. NIH-anslag/kontrakt)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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