Viewing Study NCT06372275



Ignite Creation Date: 2024-05-06 @ 8:25 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06372275
Status: RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-03-28

Brief Title: Investigating Two Prototype Mobile App Interventions to Increase Physical Activity
Sponsor: Mississippi State University
Organization: Mississippi State University

Study Overview

Official Title: Reframing Health Behavior Change A Randomized Controlled Trial of a Relational Frame Theory RFT-Informed Values Intervention for Health
Status: RECRUITING
Status Verified Date: 2024-07
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: This randomized control trial aims to investigate whether writing about personal values helps enhance motivation to engage in physical activity relative to general self-reflective writing This study will help to 1 assess whether values clarification leads to increased motivation to engage in physical activity greater stability in motivation and improvements in engagement in physical activity and valued action relative to engaging in self-reflection 2 determine if the impact of values clarification on these outcomes vary depending on context eg positivenegative affect psychological inflexibility stressful events 3 explore whether values clarification procedures that employ distinct relational frames hierarchical conditional distinction and deictic differentially impact motivation to engage in physical activity and daily engagement in physical activity and 4 explore whether the impact of values clarification vary depending on baseline self-compassion andor intrinsicextrinsic motivation
Detailed Description: This randomized control trial study aims to investigate the efficacy of a values clarification prototype mobile application intervention in increasing physical activity and enhancing motivation to exercise in a general adult sample Participants will be recruited using a variety of recruitment methods eg Google Ads posts on relevant online groups such as Facebook groups posting flyers and provider referrals Interested participants will first complete an online pre-screening asking whether they are between the ages of 18 and 65 reside in the United States want to increase their physical activity own a device that can receive text messages and have reliable internet access Participants will also be asked about why they want to participate in the study about their current level of physical activity and how they hope to change it and about how they learned about the study Those who meet the eligibility criteria in the pre-screening will be directed to review an online informed consent form Those who indicate that they consent will be directed to provide their contact information name email and phone number A trained research assistant will call the participant to ask additional screening questions assessing all exclusion criteria listed later in this registration Eligible participants at this stage will be redirected to complete a baseline survey and then be randomly assigned to either the 1 Experimental group with the values clarification mobile application or 2 the control group with the self-reflection mobile application Participants will have access to the app hosted on Qualtrics for 28 days They will first complete a tutorial and then begin completing the daily surveys in addition to the writing prompts Participants will receive daily text message reminders to use the app at a time that they specify Four weeks after baseline participants will be asked to complete a post-treatment survey and eight weeks after baseline participants will be asked to complete a final follow-up survey Participants will be given the opportunity to use the alternative app at the end of the study

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