NCT07570303

Brief Summary

Physical inactivity increases substantially after age 60 and represents a major public health challenge in older adults, as it is linked to increased risk of functional and cognitive decline and aging problems. Walking is one of the most accessible and recommended forms of light-to-moderate physical activity for this population. However, promoting sustained engagement in walking remains difficult, as traditional informational approaches often fail to activate personally meaningful motivations. This study tests whether persuasive affective messages can promote walking by leveraging self-continuity, meaning the use of autobiographical memory to maintain the sense of being the same person across time and contexts, connecting the past, present, and future self. Self-continuity is associated with psychological resources such as self-esteem, self-efficacy, and a sense of meaning in life. The affective mechanism that sustains self-continuity is nostalgia: both promote emotional and behavioral regulation and support goal achievement. Building on this framework, the present trial examines whether activating feelings of self-continuity and positive nostalgic memories can strengthen older adults' motivation to engage in walking behavior. In addition, the study investigates whether combining self-continuity messaging with a self-regulation strategy (daily step monitoring) enhances intervention effectiveness. Self-monitoring is a well-established behavioral technique that supports goal pursuit by increasing awareness and feedback. Using a 4-arm randomised controlled factorial design, the study compares the effects of self-continuity messages, step-monitoring reminders, their combination, and an active control condition on walking behaviour and its psychological determinants. A national sample of 1,000 Italian adults aged 65-74, recruited through a certified panel provider (Ipsos) and balanced for age, gender, and geographic region, will be randomly assigned to one of the four conditions. All participants will receive one message per day through a mobile application over a 14-day period. Participants in the step-monitoring conditions will also be asked to track and report their daily step count using a pedometer application. Behavioral, psychological, and process measures will be collected at baseline, post-intervention, and follow-up. The study therefore aims to provide experimental evidence on the role of self-continuity as a motivational driver of health behaviour change, and to clarify whether combining affective and self-regulatory strategies enhances intervention effectiveness in older adults.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

April 30, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 6, 2026

Completed
26 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
Last Updated

June 12, 2026

Status Verified

June 1, 2026

Enrollment Period

2 months

First QC Date

April 30, 2026

Last Update Submit

June 10, 2026

Conditions

Keywords

health behaviour changephysical activitywalkingolder adultspersuasive communicationmessagesself-monitoringself-continuity

Outcome Measures

Primary Outcomes (3)

  • Change from Baseline in Self-Reported Walking Frequency and Duration at 2-Week Post-Intervention and 4-Week Follow-up

    Assessed by International Physical Activity Questionnaire - Short Version (IPAQ). Higher scores (mean daily time spent in walking activities, number of days per week with walking activity, and mean time spent in walking activities multiplied by the number of days per week with walking activity) indicate greater self-reported walking activity over the past week and in a usual week.

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Self-Reported Walking Intensity at 2-Week Post-Intervention and 4-Week Follow-up

    Assessed by International Physical Activity Questionnaire - Short Version (IPAQ). Higher scores indicate greater self-reported walking intensity over the past week and in a usual week, with 3 ordinal response options: slow, moderate, and vigorous intensity.

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Daily Step Count at 2-Week Post-Intervention as Measured Via Pedometer App

    Higher self-reported step counts indicate greater walking activity over the past week and in a usual week.

    Baseline and 2 weeks

Secondary Outcomes (13)

  • Change from Baseline in Self-Reported Sedentary Behaviour Duration at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Self-Reported Light Physical Activity Frequency and Duration at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Self-Reported Moderate Physical Activity Frequency and Duration at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Self-Reported Vigorous Physical Activity Frequency and Duration at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Pedometer Usage and Usage Frequency (Past Week) at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • +8 more secondary outcomes

Other Outcomes (5)

  • Change from Baseline in Self-Continuity at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in State Nostalgia at 2-Week Post-Intervention and 4-Week Follow-up

    Baseline and 2 weeks and 4 weeks

  • Change from Baseline in Temporal Comparison at 2-Week Post-Intervention

    Baseline and 2 weeks

  • +2 more other outcomes

Study Arms (4)

Control

OTHER

Participants assigned to this arm will receive daily messages about the benefits of recommended daily water intake via the PsyMe app over 14 days.

Behavioral: Water intake messages

Self-continuity

EXPERIMENTAL

Participants assigned to this arm will receive daily messages via the PsyMe app over 14 days. These messages are designed to prompt recall of personally relevant past experiences and to promote walking behavior.

Behavioral: Self-continuity prompts

Step-monitoring

ACTIVE COMPARATOR

Participants assigned to this arm will receive daily reminders to monitor and record their step count through a step-tracking application via the PsyMe app over 14 days.

Behavioral: Step-monitoring reminders

Self-continuity + Step-monitoring

EXPERIMENTAL

Participants assigned to this arm will receive daily messages via the PsyMe app over 14 days. These messages combine prompts recalling relevant past experiences and promoting walking behavior with reminders to monitor and record their daily step count.

Behavioral: Self-continuity promptsBehavioral: Step-monitoring reminders

Interventions

The Day 1 introductory message presents a daily walking goal consistent with WHO recommendations and informs participants that subsequent messages describe the benefits of walking. Participants will be encouraged to pursue the physical activity goal according to their individual capabilities. Messages delivered from Day 2 to Day 13 aim to activate different positive nostalgic experiences related to walking and movement, including past memories, emotions, bodily sensations, personal values, and self-concepts. The messages link walking behaviour to such positive experiences using counterfactual formulations (e.g., "If you walk a little more today, you may reconnect with sensations your body knows well."). Message openings vary and include exclamatory statements, memory prompts, or rhetorical questions. The Day 14 message concludes the intervention.

Self-continuitySelf-continuity + Step-monitoring

The Day 1 introductory message presents a daily walking goal consistent with WHO recommendations and informs participants that subsequent messages prompt them to monitor their daily step count. Participants will be encouraged to pursue the physical activity goal according to their individual capabilities. Messages delivered from Day 2 to Day 13 provide reminders to monitor step counts throughout the day using the pedometer app and to record the total number of daily steps in PsyMe at the end of the day (e.g., "During the day, monitor your step count using the pedometer app. This evening, record the total number of steps in the app."). The Day 14 message concludes the intervention.

Self-continuity + Step-monitoringStep-monitoring

The Day 1 introductory message presents a daily water-intake goal consistent with standard recommendations and informs participants that subsequent messages describe the benefits of adequate hydration. Participants will be encouraged to pursue the goal according to their individual capabilities. Messages delivered from Day 2 to Day 13 provide brief information about different beneficial effects of adequate water intake and link hydration to each outcome using counterfactual formulations (e.g., "If you drink the recommended amount of water today, you may support your energy levels and help prevent lapses in concentration"). Message openings vary and include exclamatory statements, memory prompts, or rhetorical questions. The Day 14 message concludes the intervention.

Control

Eligibility Criteria

Age65 Years - 74 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • Age between 65 and 74 years
  • Willingness and ability to install and use the mobile applications required for study participation
  • Sufficient proficiency in the Italian language to understand study materials and complete the questionnaires.

You may not qualify if:

  • \- Physical disabilities or medical conditions that preclude engagement in light to moderate physical activity, specifically:
  • medical advice or prescription prohibiting engagement in light to moderate physical activity, assessed via a close-ended screening question;
  • positive screening on a study specific close-ended question assessing ability to perform physical activity;
  • positive screening on the adapted revised Physical Activity Readiness Questionnaire (rPAR-Q), indicating that participant may be unsafe.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Catholic University of the Sacred Heart (Milan)

Milan, Milan, 20123, Italy

Location

Related Publications (30)

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    BACKGROUND
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    PMID: 31073341BACKGROUND
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MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Patrizia Catellani, Social Psychology

    Catholic University, Italy

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Patrizia Catellani, PhD in Social Psychology

CONTACT

Valentina Carfora, PhD in Social Psychology

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
FACTORIAL
Model Details: The study is a randomized controlled trial with four parallel arms and allocation ratio 1:1:1:1. Participants will be recruited through a certified panel provider on the basis of eligibility criteria, and randomly assigned to one of four conditions: control, self-continuity, step-monitoring, or self-continuity + step-monitoring. Randomization will be implemented by the panel provider after informed consent is obtained through the delivery of access codes that direct participants to an arm-specific version of PsyMe. The intervention will last 14 days with one message delivered via the PsyMe app every day at the same hour. The content of the messages varies depending on the condition. Self-report data will be collected via questionnaires uploaded on Qualtrics and administered through the PsyMe app at three time points: baseline (T1, before the start of messaging intervention), post-intervention (T2, immediately after the 14-day messaging period), and follow-up (2 weeks after T2).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Full Professor

Study Record Dates

First Submitted

April 30, 2026

First Posted

May 6, 2026

Study Start

June 1, 2026

Primary Completion

August 1, 2026

Study Completion

August 1, 2026

Last Updated

June 12, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will share
Time Frame
They will be made available before

Locations