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Eine Studie entspricht den Filterkriterien
Kartenansicht
Adherence to Different Exercise Interventions
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT06024577 ist eine interventionsstudie zur Untersuchung von Exercise Adherence und hat den Status offene rekrutierung. Die Studie startete am 18. August 2023 und soll 60 Teilnehmer aufnehmen. Durchgeführt von California Polytechnic State University-San Luis Obispo ist der Abschluss für 1. Juli 2028 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 6. September 2023 aktualisiert.
Kurzbeschreibung
Only 50% of sedentary adults that start an exercise training program adhere to the program after 6 months. Exercise variety may improve adherence. The goal of this study is to examine different exercise interventions that include a variety of exercise on adherence.
Ausführliche Beschreibung
Regular exercise, in the form of walking 150 minutes per week, is widely regarded as having many health and fitness benefits. Despite these well-known benefits, adherence to exercise interventions is extremely low. When sedentary adults start an exercise training program only 50% adhere to the program and meet the national recommendations of 150 minutes per week. A possible explanation of the low adherence is that most adults only walk for exercise, and that providing a variety of exercise may increase adherence. Preliminary observational data show that a variety of exercise may increase weekly exercise expenditure compared to other interventions. The overall objective of this study is to investigate the feasibility, adherence, and acceptability of different exercise interventions including 1) walk intervention, 2) variety intervention, and 3) progressive intervention (see below for description).
Offizieller Titel
Aherence to Different Exercise Interventions
Erkrankungen
Exercise AdherenceWeitere Studien-IDs
- 2023-152
NCT-Nummer
Studienbeginn (tatsächlich)
2023-08-18
Zuletzt aktualisiert
2023-09-06
Studienende (vorauss.)
2028-07
Geplante Rekrutierung
60
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Offene Rekrutierung
Primäres Ziel
Behandlung
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Einfach verblindet
Studienarme/Interventionen
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
Aktives VergleichspräparatWalking Participants prescribed 150 minutes/week of moderate to vigorous walking. | Gehen Prescribed 150 minutes per week of moderate to vigorous walking. |
ExperimentellVariety Participants prescribed 150 minutes/week of moderate to vigorous variety of exercise. Each week participants will be prescribed a single different exercise (variety) which will include cycling, walking/jogging, yoga/Pilates, and cross-training. | Variety Prescribed 150 minutes per week of moderate to vigorous variety of exercise. Each week participants are randomly asked to participate in cycling, walking/jogging, yoga/Pilates, or cross-training. |
ExperimentellProgressive Participants prescribed 150 minutes/week of moderate to vigorous exercise. The exercises include cycling, walking/jogging, yoga/Pilates, and cross-training, and each week another exercise will be added to the list of options for participants. Participants may choose from the list of exercise. They do not have to do them all, and they can do as much or little (none) of whatever they choose. | Progressive Prescribed 150 minutes per week of moderate to vigorous progressive variety of exercise. Each week participants are randomly asked to participate in cycling, walking/jogging, yoga/Pilates, or cross-training. Participants can choose which exercise they want to do, and can do as much or little as they want. |
Hauptergebnismessungen
Nebenergebnismessungen
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Adherence to exercise intervention | Adherence is assessed as meeting or exceeding 150 minutes per week of moderate to vigorous exercise | Change from baseline at 1-week, 2-weeks, 3-weeks, and 4-weeks |
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Acceptability of intervention | Participants will complete a survey on acceptability at the end of the exercise intervention | Acceptability at 4-weeks |
Body Weight | Body weight will be measured at baseline and 4-weeks | Change in body weight from baseline to 4-weeks |
Eignungskriterien
Zugelassene Altersgruppen
Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle
Akzeptiert gesunde Freiwillige
Ja
- 18-40 years old
- Sedentary (<1 hour per week of exercise)
- BMI 18.5 to 40 kg/m2
- Adults with diagnosed cardiovascular, diabetes, renal, or any other metabolic disease determined by Health and Fitness History questionnaire.
- Any other disability, ailment, or physical characteristics that may hinder the ability to participate in regular exercise determined by Health and Fitness History questionnaire.
- Participating in other studies that would interfere with their ability to safely complete the exercise protocols.
- Pregnant or trying to become pregnant, and peri-menopausal or post-menopausal women.
- History of smoking within the last 6 months
- Any other vulnerable population (children <18, pregnant women, prisoners, etc.)
California Polytechnic State University-San Luis ObispoVerantwortliche Partei
Todd Hagobian, Hauptprüfer, Chair and Professor, California Polytechnic State University-San Luis Obispo
Zentrale Studienkontakte
Kontakt: Todd Hagobian, PhD, 8057567511, [email protected]
Kontakt: Adam Seal, PhD, 8057562545, [email protected]
1 Studienstandorte in 1 Ländern
California
California Polytechnic State University, San Luis Obispo, California, 93407, United States
Eric Benson, Kontakt, 805-756-7525, [email protected]
Offene Rekrutierung