Roybal Via Habit Formation
Via Habit
Automata Modeling Approach to Identify and Pilot-Test Receptive Windows for Physical Activity Habit Formation in Midlife Adults
1 other identifier
interventional
10
1 country
1
Brief Summary
This pilot study will develop and evaluate ViaHabit, a personalized walking intervention designed to promote physical activity habit formation among sedentary midlife adults (ages 45-65). During an initial 2-week observation period, participants' daily routines will be characterized using data collected from wearable devices, smartphones, and digital calendars. Personalized models will identify routine transitions, defined as periods between everyday activities, that may serve as receptive opportunities for initiating physical activity. Participants will then complete a 4-week intervention in which they create individualized "if-then" action plans linking routine transitions to a 15-minute brisk walk and receive automated smartwatch prompts at selected cue times. The study will assess the feasibility and acceptability of identifying routine transitions and delivering timely physical activity prompts, while exploring changes in walking behavior, habit strength, and physical activity engagement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 9, 2026
CompletedFirst Posted
Study publicly available on registry
September 29, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2027
September 29, 2026
August 1, 2026
7 months
September 9, 2026
September 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Feasibliity of the ViaHabit Intervention - Recruitment
Feasibility will be assessed by participant recruitment rates.
Week 8 (end of intervention)
Feasibliity of the ViaHabit Intervention - Retention
Feasibility will be assessed by participant retention rates.
Week 8 (end of intervention)
Feasibliity of the ViaHabit Intervention - Data Collection
Feasibility will be assessed by participant completion of Phase 1 data collection.
Week 8 (end of intervention)
Secondary Outcomes (1)
Habit Strength for Walking
Baseline and weekly during the 4 week intervention period through Week 8
Study Arms (1)
ViaHabit Intervention
EXPERIMENTALParticipants complete a 2-week observation period during which individualized routine models are developed using wearable, smartphone, and calendar data, followed by a 4-week ViaHabit intervention consisting of routine-transition cue selection, if-then action planning, and automated smartwatch prompts to support initiation of 15-minute brisk walks.
Interventions
ViaHabit is a personalized, cue-based walking intervention designed to promote physical activity habit formation in sedentary midlife adults. Following a 2-week observation period, individualized routine models are developed using data collected from wearable devices, smartphones, and digital calendars. Participants then complete a coaching session to identify up to two routine transitions that can serve as cues for physical activity and develop personalized if-then action plans linking each cue to a 15-minute brisk walk. During the 4-week intervention period, automated smartwatch notifications are delivered at the selected routine-transition cues to increase cue salience and support initiation of walking behavior. The intervention aims to strengthen cue-behavior associations through repeated pairing of routine completion cues with walking, thereby increasing behavioral automaticity and physical activity participation.
Eligibility Criteria
You may qualify if:
- Age 45 to 65 years.
- Reports no leisure-time physical activity during the past month and engages in \<400 MET-minutes/week of physical activity as assessed by the IPAQ-Short Form.
- Has competing role demands, defined as ≥10 hours/week of paid work, caregiving, parenting, or volunteer activities.
- Owns an iPhone (iOS smartphone) with reliable internet access and is willing to use study-related mobile applications and wearable devices.
- Able to walk without assistance.
- Uses, or is willing to use, a digital calendar application and share de-identified event timing data with the study team.
- Able to understand study procedures and provide informed consent.
You may not qualify if:
- Plans to relocate or engage in extended travel during the next 3 months.
- Pregnant or planning to become pregnant during the study period.
- Currently participating in another physical activity or behavioral intervention study.
- Has a medical condition that may limit safe participation in walking, impair the ability to provide informed consent, or interfere with study adherence.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Penn State Universitycollaborator
- Louisiana State University and A&M Collegelead
Study Sites (1)
Louisiana State University School of Kinesiology
Baton Rouge, Louisiana, 70803, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
September 9, 2026
First Posted
September 29, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
April 30, 2027
Study Completion (Estimated)
June 30, 2027
Last Updated
September 29, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share