Viewing Study NCT05285748



Ignite Creation Date: 2024-05-06 @ 5:22 PM
Last Modification Date: 2024-10-26 @ 2:27 PM
Study NCT ID: NCT05285748
Status: RECRUITING
Last Update Posted: 2022-07-20
First Post: 2022-02-23

Brief Title: Comparing Self-paced Versus Moderate Intensity Physical Activity Recommendation for Midlife Adults
Sponsor: Brown University
Organization: Brown University

Study Overview

Official Title: Comparing a Recommendation for Self-paced Versus Moderate Intensity Physical Activity for Midlife Adults an RCT
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: We will randomly assign blocked on Gender female male other body mass index BMI overweight 25 BMI 30 or obese 30 BMI 40 and pain status chronic pain vs not adults ages 50-64 into either a self-selected intensity ie SELF-PACED or b prescribed moderate intensity ie PRESCRIBED conditions Prior to randomization persons responding to our ads will participate in the following 1 telephone screening with the study research assistant RA to establish eligibility 2 an orientation session to obtain more information about the study and after providing informed consent 3 baseline assessment and screening bodyweight maximal fitness test dietary intake and questionnaires to assess potential covariates Prior to randomization the RA will give participants an accelerometer to assess baseline physical activity PA behavior over a one-week period Participants will then be randomized to one of the two study conditions Following randomization all participants will receive our theory-based PA promotion intervention to help them overcome barriers to regular PA All participants will be given chest strap heart rate HR monitors and instructions on wrist palpation Follow-up assessments will consist of accelerometry for one-week periods at months 3 6 9 and 12 ecological momentary assessment EMA throughout the 12 months and bodyweight at 3-month intervals
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
F32AG074680 NIH None httpsreporternihgovquickSearchF32AG074680