Effects of a Digital Micro-Movement Nudge Intervention on Well-Being and Academic Outcomes in College Students
1 other identifier
interventional
200
1 country
1
Brief Summary
The goal of this randomized controlled study is to learn whether a 21-day physical resilience (movement-based) program can improve mental well-being, emotional regulation, and academic functioning in university students. The main questions it aims to answer are: Does participation in a 21-day physical resilience program improve students' well-being (e.g., depression, anxiety, stress, affect, life satisfaction, and perceived health)? Does the program improve students' academic and self-regulatory outcomes (e.g., engagement, burnout, procrastination, productivity, emotion regulation, coping, and self-control capacity)? Researchers will compare students who complete the physical resilience program immediately to students in a waitlist control group to see whether participation in the program leads to greater improvements in well-being and academic-related outcomes. Participants will: Sign up online and provide informed consent Be randomly assigned to either the intervention group or a waitlist control group Receive daily micro-movement tasks and reminders via Telegram for 21 days (intervention group) Complete online questionnaire surveys at baseline, post-intervention, and a 2-week follow-up
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 6, 2026
CompletedFirst Submitted
Initial submission to the registry
February 19, 2026
CompletedFirst Posted
Study publicly available on registry
March 5, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 18, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 18, 2026
CompletedMarch 5, 2026
February 1, 2026
1 month
February 19, 2026
February 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
State anxiety
State anxiety will be assessed using the 6-item Spielberger State-Trait Anxiety Inventory STAI-6 (Marteau \& Bekker, 1992). Six items (e.g., "I was worried these past 2 weeks.") rated from 1 (Not at all) to 4 (Very much so) will be averaged for a composite score. Higher scores indicate greater levels of anxiety.
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
Procrastination
Procrastination will be assessed using six items from the Irrational Procrastination Scale (Steel, 2002), such as "At the end of these past 2 weeks, I know I could have spent the time this week better." Participants will respond on a 1-5 scale (1 = Very seldom or not true of me, 5 = Very often true, or true with me), and higher average scores indicate higher levels of procrastination.
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
Secondary Outcomes (13)
Productivity
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
Study Burnout
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
Study Engagement
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
Implementation intention
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
Goal Progress
Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks
- +8 more secondary outcomes
Study Arms (2)
Intervention group
EXPERIMENTALWaitlist Control
NO INTERVENTIONInterventions
The intervention is a 21-day, digitally delivered physical resilience program consisting of daily, brief, movement-based activities designed to support mental well-being and academic functioning in university students. The program includes low-intensity physical movement, breathing exercises, and body-based regulation practices that can be completed independently without specialized equipment or prior physical training. Participants assigned to the intervention group receive one structured movement task per day for 21 consecutive days. Tasks are delivered via a Telegram channel, accompanied by brief digital reminders to prompt engagement. Each task is designed to be short in duration, flexible in timing, and feasible within daily routines, emphasizing consistency rather than physical exertion or performance. The intervention is self-guided and asynchronous, with no in-person contact, live sessions, or direct supervision.
Eligibility Criteria
You may qualify if:
- Student of Singapore Management University
- Uses Telegram
You may not qualify if:
- Below 18 Years Old
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Singapore Management University, Online
Singapore, Singapore
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Tracy Chen Xi, PhD Candidate, Principal Investigator, Singapore Management University
Study Record Dates
First Submitted
February 19, 2026
First Posted
March 5, 2026
Study Start
February 6, 2026
Primary Completion
March 18, 2026
Study Completion
March 18, 2026
Last Updated
March 5, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share