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NCT Number: NCT07832097

Effectiveness of a Smartphone Chatbot to Improve Exercise Adherence in Older Adults

This randomized controlled trial aims to evaluate the effectiveness of a smartphone-based chatbot in improving adherence to a 12-week home-based multicomponent exercise program in community-dwelling older adults. Participants will be randomly assigned to receive either a chatbot-supported exercise program delivered through Telegram or an equivalent paper-based exercise program. Both groups will perform the same exercise program, including strength, balance, flexibility, and walking exercises. The primary outcome is exercise adherence. Secondary outcomes include physical function, physical activity, participant satisfaction, usability of the chatbot, and adverse events. The study seeks to determine whether chatbot-based support can enhance adherence and improve health outcomes in older adults.

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Key information

Age range

59 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Population aging is associated with declines in physical function, mobility, and independence. Home-based multicomponent exercise programs are effective strategies to maintain physical function and reduce the risk of disability in older adults; however, adherence to exercise programs remains a major challenge, particularly when exercises are performed without direct supervision. Effectiveness of a Smartphone-Based Chatbot on Adherence to a Home-Based Multicomponent Exercise Program and Physical Function in Older Adults: A Randomized Controlled Trial addresses this challenge by evaluating a digital intervention specifically designed to support exercise adherence.

This study is a two-arm, parallel-group randomized controlled trial conducted in community-dwelling adults aged 60 years and older. Participants are randomly allocated in a 1:1 ratio to either a chatbot-supported exercise program or a paper-based exercise program. Both groups receive the same 12-week home-based multicomponent exercise program, consisting of three exercise sessions per week. The intervention includes strength, balance, flexibility, and walking exercises with a predefined progression throughout the program.

Participants assigned to the intervention group receive exercise prescriptions through a Telegram-based chatbot. In addition to delivering the exercise program, the chatbot provides instructional videos, automated reminders, exercise monitoring, adherence tracking, scheduling adjustments, and feedback based on participants' reported exercise completion. Participants allocated to the control group receive the same exercise program in a printed booklet together with a paper calendar for recording completed sessions. Both groups receive standardized follow-up telephone calls during the intervention period.

The primary outcome is exercise adherence, defined as the percentage of prescribed exercise sessions completed during the 12-week intervention. Participants are also classified according to whether they achieve at least 80% adherence to the prescribed sessions. Secondary outcomes include physical function assessed using the Short Physical Performance Battery (SPPB), 4-meter walking test, Five Times Sit-to-Stand Test (FTSST), and Timed Up and Go (TUG) test. Additional outcomes include physical activity measured with the International Physical Activity Questionnaire for Older Adults (IPAQ-E), participant satisfaction, perceived usability of the chatbot, and adverse events.

The study will provide evidence regarding the effectiveness of chatbot-supported exercise interventions for promoting adherence to home-based exercise programs among older adults. If effective, this approach may represent a scalable and accessible strategy to support healthy aging and the implementation of exercise programs in community settings.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Community-dwelling adults aged 60 years or older.
  • Living independently in the community.
  • Ownership and regular use of a smartphone.
  • Familiarity with at least one instant messaging application and ability to access it at least three times per week.
  • Ability to understand study procedures and instructions.
  • Ability to provide written informed consent.
  • Ability to safely perform a home-based exercise program.

Exclusion criteria

  • Absolute contraindication to physical exercise.
  • Inability to understand study instructions.
  • Inability to read and/or write.
  • Uncontrolled neurological conditions that may compromise safe participation in exercise.
  • Uncontrolled cardiovascular conditions that may compromise safe participation in exercise.
  • Any medical condition judged by the investigators to prevent safe participation in the study.

Treatment and study plan

Chatbot-Supported Home-Based Exercise Program

Behavioral

A 12-week home-based multicomponent exercise program delivered through a Telegram-based chatbot. The program includes strength, balance, flexibility, and walking exercises performed three times per week. The chatbot provides exercise prescriptions, instructional videos, automated reminders, adherence monitoring, scheduling adjustments, and feedback to support exercise participation.

Other names: Telegram-Based Exercise Chatbot

Paper-Based Home Exercise Program Mostrar más líneas

Behavioral

A 12-week home-based multicomponent exercise program delivered in a printed booklet. The program includes strength, balance, flexibility, and walking exercises performed three times per week with the same content and progression as the experimental intervention. Participants record exercise completion using a paper calendar and do not receive chatbot-based reminders, monitoring, or feedback.

Primary outcomes

  1. Exercise Adherence

    Time frame: 12 weeks

    Exercise adherence will be measured as the percentage of the 36 prescribed exercise sessions completed during the 12-week intervention period. Adherence will be calculated from participant exercise records and expressed as a continuous percentage value.

Secondary outcomes

  1. Adherent Participants

    Time frame: 12 weeks

    Number and proportion of participants completing at least 80% of the prescribed exercise sessions during the intervention period.

  2. Short Physical Performance Battery (SPPB)

    Time frame: Baseline and 12 weeks

    Physical function assessed using the Short Physical Performance Battery. Scores range from 0 to 12, with higher scores indicating better physical performance.

  3. Timed Up and Go Test (TUG)

    Time frame: Baseline and 12 weeks

    Mobility assessed as the time required to stand up from a chair, walk 3 meters, turn, return, and sit down.

  4. Physical Activity Level

    Time frame: Baseline and 12 weeks

    Physical activity measured using the International Physical Activity Questionnaire for Older Adults (IPAQ-E), expressed as MET-minutes per week.

  5. Participant Satisfaction

    Time frame: 12 weeks

    Satisfaction with the intervention measured using the Client Satisfaction Questionnaire-8 (CSQ-8).

  6. Chatbot Usability

    Time frame: 12 weeks

    perceived usability of the chatbot measured using the System Usability Scale (SUS). Assessed only in the chatbot group.

Sponsors and collaborators

Lead sponsor

University of Valencia

Other

Registry information

Official study title

Effectiveness of a Smartphone-Based Chatbot on Adherence to a Home-Based Multicomponent Exercise Program and Physical Function in Older Adults: A Randomized Controlled Trial

Acronym: EXEBOT

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 21, 2026
Registry last updated
Sep 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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