Trial Radar IA | ||
|---|---|---|
Lo studio clinico NCT05472402 (LADIES Online) per Comportamento sedentario, Lack of Physical Activity, Inattività fisica è attivo, non in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui. | ||
Un studio corrisponde ai criteri del filtro
Vista a schede
Feasibility and Acceptability of an Online Program to Promote Physical Activity Among Black Women (LADIES Online)
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT05472402 (LADIES Online) è uno studio interventistico per Comportamento sedentario, Lack of Physical Activity, Inattività fisica, attualmente attivo, non in arruolamento. Avviato il 22 maggio 2022, prevede di arruolare 60 partecipanti. Sotto la guida di Gramercy Research Group, dovrebbe concludersi entro il 30 novembre 2025. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 19 aprile 2024.
Sommario breve
This study will identify strategies for modifying a physical activity intervention, previously delivered in a face-to-face format, for online implementation.
Descrizione dettagliata
Research demonstrates the health-related benefits of participation in daily physical activity (PA), including prevention and treatment of chronic diseases. Despite this knowledge, the majority of US adults, particularly black women, do not achieve recommended levels of PA and, consequently, have higher rates of related chronic disease. An efficacy study led by the proposed Principal Investigator developed and tested an in person, 10-month group-based faith-integrated (FI) or secular (SEC) PA intervention, compared with a self-guided control (SG) for black women. Both FI and SEC were superior to SG for increasing daily steps after 10 months, and FI was superior to SG for increasing daily steps 12 months post intervention. Barriers to program participation noted by participants included childcare and work responsibilities and proximity to the group meeting location. The 2018 PA Guidelines Advisory Committee Scientific Report highlighted the need for effective strategies to promote PA, including internet-delivered interventions which have demonstrated strong evidence for effectiveness at increasing PA levels. Limited data exist regarding the efficacy of internet-delivered interventions in racial/ethnic minority groups. Online delivery of our evidence-based program may increase reach and address known barriers to PA program participation in black women. This project will explore strategies for adapting the program for web-based delivery of the existing curriculum. R21 phase aims are: Aim 1: Solicit input from individuals representative of the population of focus to inform the translation of the FI curriculum for online use; Aim 2: Use the knowledge gathered in Aim 1 to adapt existing FI and SG curricula for online use; Aim 3: Assess acceptability of the online curricula in an advisory group similar to the target population. Investigators will conduct focus groups with black women to understand factors that would influence online delivery of the curriculum. A 12-member advisory group will be convened to assist with developing materials/strategies to adapt the curriculum for online delivery. In an iterative approach where material is tested, refined, and retested until complete, investigators will engage the advisory group in feasibility testing of the online curriculum
Titolo ufficiale
Feasibility and Acceptability of an Online Program to Promote Physical Activity Among Black Women
Condizioni
Comportamento sedentarioLack of Physical ActivityInattività fisicaAltri ID dello studio
- LADIES Online
- R21AG070657 (Sovvenzione/Contratto NIH (USA))
Numero NCT
Data di inizio (effettiva)
2022-05-22
Ultimo aggiornamento pubblicato
2024-04-19
Data di completamento (stimata)
2025-11-30
Arruolamento (previsto)
60
Tipo di studio
Interventistico
FASE
N.D.
Stato
Attivo, non in arruolamento
Scopo principale
Altro
Allocazione
Randomizzato
Modello di intervento
In parallelo
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
SperimentaleLADIES online intervention (R33 phase) Participants will include 30 women who will be randomized to receive six (6) months of online group-based intervention sessions that teach participants how to increase physical activity levels. | LADIES Online Intervention (R33 Phase) Participants will participate weekly online group sessions over 6 months. Participants will also receive access to written intervention materials, access to an online walking program, and access to weekly podcasts that are aligned with the intervention sessions and that support physical activity lessons with biblical scriptures. |
Comparatore placeboLADIES online control (R33 phase) Participants will include 30 women who will be randomized to receive self-guided materials that teach participants how to increase physical activity levels. Placebo comparator participants will receive their materials via the online platform. | LADIES Online Control (R33 Phase) Participants will receive online access to a written self-guided curriculum that is self-paced and teaches participants how to increase physical activity. Participants will be encouraged to complete the self-guided curriculum within 6 months. |
Esito primario
Esito secondario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Daily step counts | Daily walking over 14 consecutive days | Baseline and immediately post intervention |
Bouts of moderate-to-vigorous physical activity | Daily bouts over 14 consecutive days using a wrist-worn accelerometer | Baseline and immediately post intervention |
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
Sedentary behavior | Daily bouts over 14 consecutive days using a wrist-worn accelerometer | Baseline and immediately post intervention |
Self-reported physical activity | Participant reported using the 7-item self-administered modifided International Physical Activity Questionnaire | Baseline and immediately post intervention |
Clinical measures | Height, weight, seated blood pressure, waist circumference | Baseline and immediately post intervention |
Criteri di eleggibilità
- self-identified female
- black/African American
- > 18 years of age
- self-reported low active (i.e., achieving < 150 minutes per week of moderate-to-vigorous physical activity)
- no physical limitations or medical conditions that would be impacted by physical activity
- own a smartphone or computer with reliable high speed internet access
- able to speak and read English fluently; 8) potentially interested in participating in an online health intervention.
Parte responsabile dello studio
Melicia Whitt-Glover, Investigatore principale, President & CEO, Gramercy Research Group
Nessun dato di contatto
1 Centri dello studio in 1 paesi
North Carolina
Gramercy Research Group, Knightdale, North Carolina, 27545, United States