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Mobility DisabilityNCT07540052

Impact of Loss Aversion Messaging and Anticipated Regret for Inaction on Exercise Adherence in Older Adults

A study testing Brief Daily At-Home Strength Training Program, Loss Aversion Messaging and Standard Adherence Reminder Messaging in people with Mobility Disability and Walking Difficulty, run by Milton S. Hershey Medical Center at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to learn if messages focused on not losing the functional benefits of exercise can help older adults with walking difficulty continue to exercise regularly. Read more about this study

Who is it for?
Ages 65 years and older
Conditions the study is for
Mobility Disability, Walking Difficulty
What is being tested?
Brief Daily At-Home Strength Training Program, Loss Aversion Messaging and Standard Adherence Reminder Messaging
Could I receive a placebo?
No, everyone receives an active treatment
How many people
148 participants
Where
1 siteUnited States
Study dates
Nov 2026to Jan 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 years and older
  • All sexes
  • No healthy volunteers
  • Older adult

Who may be able to join

  • Completed 12 months of FAST intervention

Who cannot join

  • No planned surgeries within the upcoming 4 months

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site
  • Penn State College of Medicine

    Hershey, Pennsylvania, 17033

    Jordan D Kurth, PhD, (717) 531-4417, jkurth@pennstatehealth.psu.edu

Other trials in United States

About this study

Official title: Testing the Impact of Loss Aversion Messaging and Anticipated Regret for Inaction on Exercise Adherence in Older Adults: A Randomized Pilot Trial

The goal of this clinical trial is to learn if messages focused on not losing the functional benefits of exercise can help older adults with walking difficulty continue to exercise regularly. The main questions it aims to answer are:

Do these messages make people more likely to anticipate regretting it if they do not exercise? Does more anticipated regret make it more likely they will exercise more regularly?

Read more

Researchers will compare two versions of messages to see if the content of these one of these message types is more effective than the other.

Participants will complete a daily 5-minute at home exercise program for 4 months and complete regular online surveys to track their progress and report their feelings regarding regret.

Read the detailed description

The goal of the proposed clinical trial is to identify strategies to blunt the effects of post-intervention decay in older adults with difficulty walking. While early improvements from exercise are large, they typically plateau and then decline post-intervention. This early improvement, however, creates an opportunity. Similar to daily interactions common with private companies, the investigators seek to increase the rate of conversion - that is, completing the task - while considering the improvements from engaging in exercise to be accumulated benefits. Drawing from behavioral economics, then, the investigators propose that the conversion rate to act (i.e., increase the likelihood of completing daily exercises) may be increased by using loss aversion (i.e., loss of accumulated benefits) in the form of messaging.

In this study the investigators will conduct a randomized trial among individuals (N=128) age 65 and over who have serious difficulty walking and have completed an at-home, brief strength training intervention, comparing 4 months of standard adherence reminders to standard adherence reminders supplemented with periodic loss aversion messages. The proposed trial aims to answer the questions: (1) Does the supplementation of loss aversion messaging increase anticipated regret for inaction among older adults previously enrolled in an at-home exercise program? (2) Does higher anticipated regret predict greater intention to exercise and exercise adherence post-intervention?

Being tested
Brief Daily At-Home Strength Training Program, Loss Aversion Messaging, Standard Adherence Reminder Messaging
Keywords
exercise adherence, older adults, mobility disability, walking difficulty, pilot study, randomized controlled trial
Medical subject headings
Mobility Limitation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Brief Daily At-Home Strength Training ProgramBehavioural

    FAST is a brief, daily, at-home exercise program designed for older adults with difficulty walking. The program includes 5 exercises performed for 30 seconds each, during which time participants try to complete as many repetitions as they can, followed by 30 seconds of rest.

    The 5 exercises are: chair stands, countertop pushups, aerobic steps, resistance band rows, and walking laps. Participants are sent daily reminders and links for self-monitoring their performance.

  • Loss Aversion MessagingBehavioural

    Loss aversion messages will be included with those messages in the experimental condition on a maximum of 3 out of the 7 days each week. There will be 3 themes (related to their performance of daily exercises) featured as topics for the loss aversion messages. The three themes are: 1) standing up from a chair (i.e., chair stands), 2) going up and down stairs (i.e., aerobic steps), and 3) walking longer distances (i.e., walking laps).

  • Standard Adherence Reminder MessagingBehavioural

    Standard reminders to perform exercise will be delivered daily.

Study groups in NCT07540052
Study groupRoleWhat they receive
Loss Aversion MessagingExperimentalStandard reminders to perform exercise will be delivered daily. Loss aversion messages will be included with those messages in the experimental condition on a maximum of 3 out of the 7 days each week. There will be 3 themes (related to their performance of daily exercises) featured as topics for the loss aversion messages. The three themes are: 1) standing up from a chair (i.e., chair stands), 2) going up and down stairs (i.e., aerobic steps), and 3) walking longer distances (i.e., walking laps).
Receives: Behavioral: Brief Daily At-Home Strength Training Program; Behavioral: Loss Aversion Messaging; Behavioral: Standard Adherence Reminder Messaging
Standard Adherence MessagingActive comparatorStandard reminders to perform exercise will be delivered daily.
Receives: Behavioral: Brief Daily At-Home Strength Training Program; Behavioral: Standard Adherence Reminder Messaging

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anticipated Regret of Inaction

    One is equivalent to definitely not anticipating regret and 8 indicates definitely anticipating regret.

    Measured: Baseline, Week 4, Week 8, Week 12, and Week 16

Secondary outcomes (2)
  1. Intention to Complete Exercise Program

    One indicates definitely not intending to complete all of the exercise program over the next week and 8 indicates definitely intending to complete all of the exercise program over the next week.

    Measured: Baseline, Week 4, Week 8, Week 12, and Week 16

  2. Adherence to Exercise Program

    A percentage of days on which the exercise program was completed (0-100%).

    Measured: Data collected daily, assessed over the 16 weeks of intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Apr 2026
  2. Study startNov 2026 (estimated)
  3. Primary completionDec 2027 (estimated)
  4. Study completionJan 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
148 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07540052
Sponsor's protocol ID
STUDY00028949
Status last verified
Aug 2026
First submitted
10 Apr 2026
Last updated
12 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Brief Daily At-Home Strength Training Program, Loss Aversion Messaging and Standard Adherence Reminder Messaging in people with Mobility Disability and Walking Difficulty, run by Milton S. Hershey Medical Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 12 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jordan D Kurth, PhD ((717) 531-4417, jkurth@pennstatehealth.psu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anticipated Regret of Inaction (time frame: Baseline, Week 4, Week 8, Week 12, and Week 16). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Aug 2026.

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