Physical PerformanceNCT07895446
Effects of AI-Generated Resistance Training on Neuromuscular Performance in Sedentary Men
A study testing Artificial Intelligence-Generated Resistance Training and Conventional Resistance Training in people with Physical Performance, run by Marmara University at 1 site in Turkey (Türkiye).
Trial summary
The goal of this clinical trial is to learn how an artificial intelligence-generated resistance training program affects muscle performance in sedentary men aged 18 to 35 years. The main questions it aims to answer are: How does an artificial intelligence-generated resistance training program affect the participants'… Read more about this study
- Who is it for?
- Ages 18 to 35 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Physical Performance
- What is being tested?
- Artificial Intelligence-Generated Resistance Training and Conventional Resistance Training
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 6 Jan 2025to 3 Mar 2025
- 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 35 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Male
- Aged between 18 and 35 years
- Sedentary lifestyle
- No participation in regular resistance training during the previous six months
- No history of orthopedic, neurological, or musculoskeletal disorders
Who cannot join
- None specified
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Health Coaching Pilates & Fitness
Istanbul, 34854
About this study
Official title: Investigation of the Effects of Artificial Intelligence-Generated Training Programs on Strength, Speed, and Power Parameters
The goal of this clinical trial is to learn how an artificial intelligence-generated resistance training program affects muscle performance in sedentary men aged 18 to 35 years. The main questions it aims to answer are:
- How does an artificial intelligence-generated resistance training program affect the participants' ability to produce force?
- How does this program compare with a resistance training program designed by a professional coach and with no structured resistance training? Researchers will compare three groups: an artificial intelligence-generated resistance training group, a coach-designed resistance training group, and a non-exercising control group.
Participants in the two training groups will complete supervised resistance training three times per week for eight weeks. Participants in the control group will not take part in structured resistance training. Researchers will measure muscle performance before and after the eight-week study period to compare changes among the three groups.
- Conditions
- Physical Performance
- Being tested
- Artificial Intelligence-Generated Resistance Training, Conventional Resistance Training
- Keywords
- Artificial Intelligence, Resistance Training, Strength, Power, Speed, Sedentary Men
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Artificial Intelligence-Generated Resistance TrainingBehavioural
An eight-week resistance training program generated using artificial intelligence. The program was implemented in the Artificial Intelligence-Generated Training Group.
Conventional Resistance TrainingBehavioural
An eight-week resistance training program developed without the use of artificial intelligence. The program was implemented in the Conventional Training Group.
| Study group | Role | What they receive |
|---|---|---|
| Artificial Intelligence-Generated Training Group | Experimental | Participants in this arm received an eight-week resistance training program generated using artificial intelligence. Receives: Behavioral: Artificial Intelligence-Generated Resistance Training |
| Conventional Training Group | Active comparator | Participants in this arm received an eight-week resistance training program developed without the use of artificial intelligence. Receives: Behavioral: Conventional Resistance Training |
| Control Group | No intervention | Participants in this arm did not participate in the resistance training intervention during the eight-week study period. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Peak Force
Peak force was assessed during maximal voluntary isometric contractions using the Beyond Power Voltra 1 system. Measurements were obtained bilaterally for the quadriceps, hamstrings, plantar flexors, and dorsiflexors.
Measured: Baseline and Week 8
Impulse (0-100 ms)
Impulse during the first 0-100 ms of maximal voluntary isometric contraction was assessed using the Beyond Power Voltra 1 system. Measurements were obtained bilaterally for the quadriceps, hamstrings, plantar flexors, and dorsiflexors.
Measured: Baseline and Week 8
Rate of Force Development (0-100 ms)
Rate of force development during the first 0-100 ms of maximal voluntary isometric contraction was assessed using the Beyond Power Voltra 1 system. Measurements were obtained bilaterally for the quadriceps, hamstrings, plantar flexors, and dorsiflexors.
Measured: Baseline and Week 8
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Oct 2026
- Study start6 Jan 2025
- Primary completion3 Mar 2025
- Study completion3 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Physical PerformanceStudies of the same condition, open and under way.
- More trials run by Marmara UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Marmara University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Eser Ağgön, PhD, Principal investigator, Marmara University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07895446
- Sponsor's protocol ID
- E-83765773-050.04-1095293
- Status last verified
- Sep 2026
- First submitted
- 19 Oct 2026
- Last updated
- 2 Nov 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data underlying the results reported in this study will be available upon reasonable request.
Study at a glance
From the registry record, last updated by the sponsor on 2 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigation of the Effects of Artificial Intelligence-Generated Training Programs on Strength, Speed, and Power Parameters
- ClinicalTrials.gov ID
- NCT07895446
- Acronym / sponsor ID
- E-83765773-050.04-1095293
- Conditions
- Physical Performance
- Keywords
- Artificial Intelligence, Resistance Training, Strength, Power, Speed, Sedentary Men
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Marmara UniversityUniversity, hospital or other
- Study start
- 6 Jan 2025 (actual)
- Primary completion
- 3 Mar 2025 (actual)
- Study completion
- 3 Mar 2025 (actual)
- First posted
- 26 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to learn how an artificial intelligence-generated resistance training program affects muscle performance in sedentary men aged 18 to 35 years. The main questions it aims to answer are:
- How does an artificial intelligence-generated resistance training program affect the participants' ability to produce force?
- How does this program compare with a resistance training program designed by a professional coach and with no structured resistance training? Researchers will compare three groups: an artificial intelligence-generated resistance training group, a coach-designed resistance training group, and a non-exercising control group.
Participants in the two training groups will complete supervised resistance training three times per week for eight weeks. Participants in the control group will not take part in structured resistance training. Researchers will measure muscle performance before and after the eight-week study period to compare changes among the three groups.
Study design
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Artificial Intelligence-Generated Training Group | Experimental | Behavioral: Artificial Intelligence-Generated Resistance TrainingParticipants in this arm received an eight-week resistance training program generated using artificial intelligence. |
| Conventional Training Group | Active comparator | Behavioral: Conventional Resistance TrainingParticipants in this arm received an eight-week resistance training program developed without the use of artificial intelligence. |
| Control Group | No intervention | –Participants in this arm did not participate in the resistance training intervention during the eight-week study period. |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- Male
- Aged between 18 and 35 years
- Sedentary lifestyle
- No participation in regular resistance training during the previous six months
- No history of orthopedic, neurological, or musculoskeletal disorders
Key exclusion criteria (1 listed)
- None specified
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Artificial Intelligence-Generated Resistance TrainingAn eight-week resistance training program generated using artificial intelligence. The program was implemented in the Artificial Intelligence-Generated Training Group. | Behavioural | Artificial Intelligence-Generated Training Group |
| Conventional Resistance TrainingAn eight-week resistance training program developed without the use of artificial intelligence. The program was implemented in the Conventional Training Group. | Behavioural | Conventional Training Group |
Primary outcome
Peak Force
Time frame: Baseline and Week 8
Peak force was assessed during maximal voluntary isometric contractions using the Beyond Power Voltra 1 system. Measurements were obtained bilaterally for the quadriceps, hamstrings, plantar flexors, and dorsiflexors.
Impulse (0-100 ms)
Time frame: Baseline and Week 8
Impulse during the first 0-100 ms of maximal voluntary isometric contraction was assessed using the Beyond Power Voltra 1 system. Measurements were obtained bilaterally for the quadriceps, hamstrings, plantar flexors, and dorsiflexors.
Rate of Force Development (0-100 ms)
Time frame: Baseline and Week 8
Rate of force development during the first 0-100 ms of maximal voluntary isometric contraction was assessed using the Beyond Power Voltra 1 system. Measurements were obtained bilaterally for the quadriceps, hamstrings, plantar flexors, and dorsiflexors.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Nov 2026.
- Individual participant dataSharing planned: Yes. De-identified individual participant data underlying the results reported in this study will be available upon reasonable request.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Eser Ağgön, PhD principal investigator
Marmara University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Artificial Intelligence-Generated Resistance Training and Conventional Resistance Training in people with Physical Performance, run by Marmara 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 5 inclusion and 1 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 2 Nov 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?
Peak Force (time frame: Baseline and Week 8). 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 2 Nov 2026.