AzTrials
AzTrials

Office WorkersNCT07242287

Flexibility Exercises, Created by AI and Humans, on Office Workers' Flexibility, Back-health and Muscle-stiffness.

A study testing AI-created exercise and Human-created exercise in people with Office Workers, run by Erzurum Technical University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

While the benefits of flexibility exercises for office workers are well known, there is no randomized controlled comparison to determine whether these exercises can be delivered more effectively and safely by a specialist or by an automated artificial intelligence algorithm. Read more about this study

Who is it for?
Ages 18 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Office Workers
What is being tested?
AI-created exercise and Human-created exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Dec 2025to 30 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

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 18 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Not have any known chronic orthopedic problems (active injuries requiring surgery or causing limited mobility).
  • Be able to walk distances of 150 meters or more without assistance.
  • Be an office worker who spends most of their working hours at a desk (at least 30 hours per week).

Who cannot join

  • Having a condition that causes acute or chronic pain related to the musculoskeletal system.
  • Having undergone major surgery within the last 6 months.
  • Experiencing a health problem during participation that would cause any physical activity restrictions.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Erzurum Technical University Health Science Faculty

    Erzurum, 25050

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of15-Minute Home-Based Flexibility Exercises Derived by Artificial Intelligence and Produced by Humans on the Overall Flexibility, Back Health, and Muscle Stiffness Levels of Office Workers: A Randomized Controlled Trial

While the benefits of flexibility exercises for office workers are well known, there is no randomized controlled comparison to determine whether these exercises can be delivered more effectively and safely by a specialist or by an automated artificial intelligence algorithm. Furthermore, considering the dynamic programming potential of artificial intelligence, determining whether this method can provide results similar to or superior to traditional methods is critical for the development of future healthcare models. The primary objective of this study is to compare the effects of 15-minute home-based flexibility exercises derived by artificial intelligence and produced by humans, administered over a 4-week period, on office workers' overall flexibility, back health, and muscle stiffness levels. This study is a two-armed, single-blind randomized controlled trial. Participants will be blinded to which group they are assigned to. This study will be respond "Are flexibility exercises generated by artificial intelligence more effective than human-generated flexibility exercises" question. During the study, participants who sign the volunteer information form and consent form and meet the inclusion criteria will be divided equally into two groups using a simple random method (coin toss):

  • Group A: Artificial Intelligence (AI)-Based Flexibility Group.
  • Group B: Human Expert-Based Flexibility Group. Intervention programs will include a standardized 15-minute flexibility exercise program will be automatically generated for each participant via Gemini, an AI-powered platform for group A, and a 15-minute program consisting of standardized flexibility exercises modified for each participant created by two qualified physiotherapists, based on calisthenic exercises (using body weight). This program will target the same muscle groups as the AI group's program and will be of similar duration. The exercise program will last a total of 4 weeks. Participants will exercise 3 days a week (Monday, Wednesday, Friday) for 15 minutes a day in their own environment.
Read the detailed description

This study will be a randomized controlled trial. The hypothesis of the study;

  • HO1: Flexibility exercises generated by artificial intelligence improve overall flexibility in office workers more than human-generated flexibility exercises.
  • HO2: Flexibility exercises generated by artificial intelligence reduce back pain levels in office workers more than human-generated flexibility exercises.
  • HO3: Flexibility exercises generated by artificial intelligence are more effective than human-generated flexibility exercises in relaxing muscle stiffness in office workers.

Office workers employed at Erzurum Technical University will be included in the study. The minimum number of participants required for the study was determined to be 21 people per group using the Gpower 3.1 (Düsseldorf, Germany) program, with a 0.05 margin of error, 95% confidence interval, and 1.03 effect size.

All participants' pre-test (baseline) and post-test measurements at the end of the 4-week intervention period will be collected under the same conditions and in the same environment. The exercises for both groups will be provided to them as a brochure after the first measurement session, and instructions on how to perform them will be given. The intervention period will last for 4 weeks. On exercise days-Monday, Wednesday, and Friday-participants will receive reminder messages via the designated online communication group to remind them to do their exercises. Participants will be asked to provide brief feedback confirming they have completed the exercises for compliance tracking.

The AI-generated flexibility exercises will consist of a 2-minute warm-up, 11 minutes of stretching and flexibility exercises (including static and dynamic stretches), and a 2-minute cool-down. Human-generated flexibility exercises will consist of a 2-minute warm-up modified from calisthenic exercises, 11 minutes of main flexibility exercises (squats, modified push-ups, planks, etc.), and a 2-minute cool-down.

In our study, a demographic data collection form will be used to evaluate demographic data, the sit-and-reach test for flexibility assessment, the Oswestry Disability Index to assess back health, and the MyotonPRO muscle tone assessment device to evaluate muscle stiffness.

All measurements will be conducted in two sessions at the Therapeutic Exercise Laboratory of Erzurum Technical University. Measurements will be taken immediately before the start of the study and after the 4-week training period. An informed consent form will be obtained from each participant, and the test procedures will be explained in detail. Measurements will be performed by an experienced physical therapist in accordance with standardized protocols. Participants will be given sufficient rest time before each test, and their safety will be ensured. The total assessment time is estimated to be 12 minutes for each participant.

The obtained data will be analyzed using the SPSS 24.0 (Statistical Package for the Social Sciences) program. At the same time, comparisons will be made by entering the norm values into the SPSS 24.0 program. The Kolmogorov-Smirnov or Shapiro-Wilk tests will be used to examine whether the data are normally distributed. Descriptive statistics (mean, standard deviation) will be used for normally distributed data. The X2 test will be used for categorical variables. The independent samples t-test will be used to compare independent groups. Non-parametric tests (e.g., Mann-Whitney U test) will be preferred for data that do not show a normal distribution. For intra-group comparisons, the paired t-test or Wilcoxon signed rank test will be used depending on the normal distribution status of the data. In all statistical analyses, the significance level will be accepted as p<0.05.

Conditions
Office Workers
Being tested
AI-created exercise, Human-created exercise
Keywords
Flexibility exercises, AI-created, Human-created, Muscle stiffness, back health, flexibility

What participants receive

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

  • AI-created exerciseOther

    Also called Flexibility exercise derived by AI

    15-minute home flexibility exercise program derived by artificial intelligence over 4 weeks

  • Human-created exerciseOther

    Also called Flexibility exercises producted by human

    15-minute home flexibility exercise program producted by human over 4 weeks

Study groups in NCT07242287
Study groupRoleWhat they receive
15-Minute Home-Based Flexibility Exercises Derived by Artificial Intelligence GroupExperimentalAn AI-powered platform called Gemini will automatically generate a standardized 15-minute flexibility exercise program for each participant. This program will include dynamic and static stretching exercises.
Receives: Other: AI-created exercise
15-Minute Home-Based Flexibility Exercises Producted by Human GroupExperimentalFor this group, a 15-minute program consisting of standardized flexibility exercises modified for each participant based on calisthenic exercises (bodyweight exercises) will be created by two qualified physical therapists. This program will target similar muscle groups and have the same duration as the AI group's program.
Receives: Other: Human-created exercise

What is being measured

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

  1. Body flexibility

    The sit-and-reach test will be used for evaluation. This test measures body flexibility and is performed on a specially developed sit-and-reach bench. Sit with both legs straight on the floor. One hand is placed on top of the other with the middle fingertips aligned. The soles of the feet are placed on the footrest of the measuring device. The subject is instructed to inhale and then, while exhaling, bend at the hips and reach forward, pushing the sliding ruler on the device. The back should be straight and the head up. Avoid jumping or rapid movements, and never stretch to the point of pain. Keep the knees straight and hold the reaching position for 2 seconds. Record the distance traveled by the sliding ruler in centimeters. Perform two trials. Record the longest distance. This is a valid and safe test.

    Measured: The change from baseline sit and reach test score at week 4.

  2. Back health

    It will be assessed using the Oswestry Disability Index. This questionnaire, which assesses back health in 10 categories, is calculated out of a total of 50 points. A high score indicates a poor prognosis.

    Measured: The change from baseline Oswestry Disability Index score at week 4.

  3. Muscle stiffness

    The MyotonPRO muscle characteristics assessment device will be used for evaluation. This device provides the ability to measure changes in muscle tone instantly and objectively. It has been developed to assess muscle tone, muscle stiffness, and muscle elasticity. It is a reliable measurement device for assessing back health. The assessment will be performed on the muscle groups most related to back health and flexibility limitations in office workers, namely the lumbar erector spinae (lower back), hamstrings (back of the thigh), and gastrocnemius medialis (calf).

    Measured: The change from baseline MyotonPRO device score at week 4.

Timeline

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

  1. First posted21 Nov 2025
  2. Study start15 Dec 2025
  3. Primary completion28 Jan 2026
  4. Study completion30 Jan 2026

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
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07242287
Sponsor's protocol ID
mehmet.sonmez2
Status last verified
Aug 2026
First submitted
17 Nov 2025
Last updated
25 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing AI-created exercise and Human-created exercise in people with Office Workers, run by Erzurum Technical University at 1 site in Turkey (Türkiye).

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 3 inclusion and 3 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: finished, as of the sponsor's last update on 25 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 Turkey (Türkiye). 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Body flexibility (time frame: The change from baseline sit and reach test score at week 4.). The study lists 3 primary outcomes in all. 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 25 Aug 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in