ClinicalTrials.gg
Enrolling by invitationNCT07390695Updated Feb 5, 2026

The Researchers Would Like to Conduct a Trial Using Gamified Exercise to Increase Cardiorespiratory Fitness and Intention to Quit Smoking Among Hardcore Smokers Who Are Also Physically Inactive.

An interventional study of Gamification of a structured exercise program in Cardiorespiratory Fitness or Endurance and Smoking Cessation, sponsored by Gadjah Mada University. Enrolling by invitation at 1 site in Indonesia. Open to male participants aged 17 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-05.

Sponsored by Gadjah Mada University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2026, 5 months ago, but the record still lists the study as enrolling by invitation.
  • Registered 3 months after the study started (first participant enrolled Sep 2025, registered Dec 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
17 Years to 45 Years
Sex
Male
01

Study summary

The goal of this quasi-experiment is to learn if a gamified exercise works to improve cardiorespiratory fitness in physically inactive hardcore smokers. It will also learn about the effects of smoking cessation. The main questions it aims to answer are:

  • Does a gamification of a structured training program improve the cardiorespiratory fitness and smoking cessation behavior among smokers?
  • Is there any mediating effect from the level of physical activity between a gamified exercise and cardiorespiratory fitness?
  • Will the smokers engage in the gamified exercise within the 12-week intervention?

This is a no-control group. The quasi-experiment will be conducted within one group (paired data).

02

Conditions studied

  • Cardiorespiratory Fitness or Endurance
  • Smoking Cessation

Keywords

  • exercise
  • gamification
  • cardiorespiratory fitness
  • smoking cessation
03

In context

Smoking Cessation

1,581 studies on the registry are indexed under Smoking Cessation; 198 are open to participants now.

This study's planned enrollment of 60 is below the median of 164 across 1,423 interventional studies indexed under Smoking Cessation.

Browse Smoking Cessation studies →

Lead sponsor

Gadjah Mada University is the lead sponsor of 63 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
17 Years to 45 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • hardcore smokers (min 20 cigarettes per day)
  • being active smokers at least 1 year
  • physically active (MET less than 600 MET minutes per week)

Exclusion criteria

Exclusion Criteria:

  • having any medical conditions that limit them to participation in a program training
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Gamification Team

    A group of 60 physically inactive hardcore smokers participated in this study using a gamified exercise within 12 12-week intervention.

    Behavioral: Gamification of a structured exercise program

Interventions

  • BehavioralGamification of a structured exercise program

    A structured exercise program with FITT-VP principles is gamified and delivered to 60 physically inactive hardcore smokers.

06

What researchers measure

Primary outcomes

  1. Estimated Maximal Oxygen Uptake (VO2Max) Measured by the Cooper 12-Minute Run Test

    Estimated cardiorespiratory fitness assessed using the Cooper 12-Minute Run Test. Participants are instructed to run or walk as far as possible within 12 minutes. The total distance covered (in meters) is used to estimate maximal oxygen uptake (VO2Max), expressed in milliliters per kilogram per minute (mL/kg/min). Higher VO2Max values indicate better cardiorespiratory fitness.

    Time frame: Baseline (Week 0) and post-intervention (Week 13)

Secondary outcomes

  1. Level of Physical Activity Measured by the World Health Organization Global Physical Activity Questionnaire (GPAQ)

    Physical activity level assessed using the World Health Organization Global Physical Activity Questionnaire (GPAQ). The GPAQ measures physical activity across work, transport, and leisure domains. Total physical activity is calculated in metabolic equivalent task minutes per week (MET-minutes/week). Higher scores indicate higher levels of physical activity.

    Time frame: Baseline (Week 0) and post-intervention (Week 13)

  2. Intention to Quit Smoking Measured by the Intention to Quit Smoking Scale (IQSS)

    Smoking cessation intention was assessed using the Intention to Quit Smoking Scale (IQSS) developed by Söyler and Yorulmaz (2024). The IQSS is a self-reported questionnaire consisting of multiple items rated on a Likert-type scale. Total scores range from 8 to 40, with higher scores indicating a stronger intention to quit smoking.

    Time frame: Baseline (Week 0) and post-intervention (Week 13)

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07390695
Lead sponsor
Gadjah Mada University
Responsible party
Ahmad Hidayat (Principal Investigator, Gadjah Mada University) — Principal investigator
First posted
Feb 5, 2026
Start date
Sep 1, 2025
Primary completion
Jun 2026 (estimated)
Completion
Sep 2026 (estimated)
Last update
Feb 5, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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