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Not yet recruitingNCT07087457FIT-MOSUpdated Jul 28, 2025

The Effect of Transtheoretical Model-Based Exercise Interventions on Increasing Physical Activity in Office Workers

An interventional study of The digital stimulus command and 5 day 30-minute walking program in Office Workers and Sedanter, sponsored by Akdeniz University. Not yet recruiting. Open to participants aged 18 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-28.

Sponsored by Akdeniz University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years to 64 Years
Sex
All
01

Study summary

This study aims to evaluate the effect of human and digital stimulus exercise interventions based on the transtheoretical model on increasing physical activity levels in sedentary office workers. In the study, which is planned to be conducted with a randomized crossover design, participants will be randomly assigned to different intervention conditions (human and digital stimulus). Interventions will be structured in accordance with the behavior change stages of individuals and will be implemented over a certain period of time. Within the scope of the study, physiological indicators such as heart rate variability will be evaluated along with physical activity level. This study is aimed to contribute to the development of evidence-based intervention models to support the physical activity habits of individuals working in an office environment.

Translated with DeepL.com (free version)

02

Conditions studied

  • Office Workers
  • Sedanter

Keywords

  • Sedentary lifestyle
  • inactivity
  • office workers
  • transthoretical model
  • digital stimuli
  • physical activity
  • hearth rate
03

In context

Sedentary Behavior

332 studies on the registry are indexed under Sedentary Behavior; 156 are open to participants now.

This study's planned enrollment of 52 is below the median of 70 across 287 interventional studies indexed under Sedentary Behavior.

Browse Sedentary Behavior studies →

Lead sponsor

Akdeniz University is the lead sponsor of 289 studies on the registry; 60 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Office workers scoring \<600 METdk/week according to the FAA survey Employees who agreed to participate in the study. Employees who are in reflection and preparation stages of TTM change.

Exclusion criteria

Exclusion Criteria:

  • Part-time workers, Pregnant women, People with health problems that may increase the risk of walking (musculoskeletal system disorders, people with advanced heart failure diagnosis (based on self-report), rheumatologic, etc.) Workers who are in not thinking, moving and sustaining stages of TTM change.
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
52 participants (estimated)

Study arms

  • Experimental
    Group A-The digital stimulus command

    The digital stimulus command: This group will receive only digital alerts for 4 weeks. Following the washout period, they will participate in a 5-day, 30-minute walking program, accompanied by a researcher, for 4 weeks.

    Behavioral: The digital stimulus command · Behavioral: 5 day 30-minute walking program

  • Experimental
    Group B- 5-day 30-minute walking program

    5 day 30-minute walking program. This group will participate in a 30-minute walking program for 5 days a week, accompanied by a researcher, for 4 weeks. Following the washout period, they will receive in the digital stimulus commands for 4 weeks.

    Behavioral: The digital stimulus command · Behavioral: 5 day 30-minute walking program

Interventions

  • BehavioralThe digital stimulus command

    The digital stimulus command: Providing information on the harms of inactivity and sedentary lifestyle on online, digital platforms. The individual will take the HRV measurement in a sitting position for 5 minutes every morning (before consuming tobacco products for smokers) as taught and will send the screenshot of the data to the researcher via WhatsApp. Ensuring that the digital stimulus commands that will remind the activity in line with TTM are followed by reminders sent to the computer screen or mobile phones. Taking a break from sitting when the command "It's time for activity" comes (taking a total of 6 breaks in the working hours of 08:30 - 17:30, 1 every 60 minutes recording the activity as "completed" in the digital diary and survey form) \*Activities of office workers other than the time they spend sitting; Recording the number of steps and activities in the office, its surroundings and in daily life in a digital diary.

  • Behavioral5 day 30-minute walking program

    5 day 30-minute walking program. This group was also defined as the human stimulus group because, in addition to the digital stimulus command, they will be invited by the researcher and will participate in the walking program with the researcher. This group will first receive the activity program and simultaneously will also receive the digital stimulus command interventions.

06

What researchers measure

Primary outcomes

  1. 1. Physical Activity Assessment

    International Physical Activity Questionnaire Short Form: The questionnaire consists of seven questions covering all types of physical activity. Physical activity levels are categorized as physically inactive, low physical activity, and adequate physical activity.

    Time frame: At baseline, in the washout period after intervention A (6th week) and after intervention B (11th week)

  2. Transtheoretic Model Scale for physical activity

    This scale has four dimensions. 1. Exercise Stages of Change: The scale consists of a single question with five options. Based on participants' responses, the exercise stage of change they are in is determined. 2. Exercise Change Processes: The scale consists of 28 items, 10 sub-dimensions, and two main processes (cognitive and behavioral). Cognitive processes include increased awareness, dramatic help/emotional revitalization, environmental reappraisal, self-reappraisal, and social liberation. Behavioral processes include contrast/opposition, helping relationships, reinforcement management, self-liberation, and stimulus control. 3. Exercise Self-Efficacy: This scale aims to assess an individual's strengths regarding exercise behavior. 4. Exercise Decision-Making Balance: Explains the cognitive factors and motivational factors that play a role in the decision-making process for the individual's exercise behavior.

    Time frame: At baseline, in the washout period after intervention A (6th week) and after intervention B (11th week)

Secondary outcomes

  1. Heart Rate Variability

    Heart Rate Variability is an important physiological indicator related to the interactions between the sympathetic and parasympathetic divisions of the autonomic nervous system. HRV, a control system used to regulate unconscious actions such as heart function, respiration, digestion, blood pressure, urination, and pupil dilation/contraction, is used to analyze the autonomic nervous system. In our study, we will use the Polar H10 Chest Strap, a widely used research tool, to determine HRV. In a validation study, linear HRV measurements obtained from the Polar H10 chest strap demonstrated strong agreement compared to ECG recordings.

    Time frame: At baseline, during the washout period after intervention A (week 6), and after intervention B (week 11)

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Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 28, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07087457
Lead sponsor
Akdeniz University
Responsible party
Sebahat Gozum (Proffesor, Akdeniz University) — Principal investigator
First posted
Jul 28, 2025
Start date
Oct 1, 2025 (estimated)
Primary completion
Dec 30, 2025 (estimated)
Completion
Jun 30, 2026 (estimated)
Last update
Jul 28, 2025

Study contacts

Sebahat GÖZÜM, Prof.Dr.
Contact
sgozum@akdeniz.edu.tr
+902423106916

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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