Healthy VolunteersSmartVibNCT07521228
Acute Effects of Smartphone-Delivered Local Vibration on Hand Sensorimotor Performance
A study testing Smartphone Local Vibration at 80 Hz, Smartphone Local Vibration at 150 Hz and Smartphone Local Vibration at 220 Hz in people with Healthy Volunteers and Vibration; Adverse Effect, run by Acibadem University at 1 site in Turkey (Türkiye).
Trial summary
This study investigates the acute effects of smartphone-delivered local vibration on hand sensorimotor performance in healthy young adults. Using a custom-developed iPhone application, three vibration frequencies (80 Hz, 150 Hz, and 220 Hz) are applied to the dominant hand in a randomized crossover design with a… Read more about this study
- Who is it for?
- Ages 18 to 25 yearsHealthy volunteers can take part
- Conditions the study is for
- Healthy Volunteers, Vibration; Adverse Effect
- What is being tested?
- Smartphone Local Vibration at 80 Hz, Smartphone Local Vibration at 150 Hz and Smartphone Local Vibration at 220 Hz
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- Apr 2026to Nov 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 25 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Healthy university students aged 18-25 years
- Willing to participate and provide written informed consent
- Able to attend three separate measurement sessions
Who cannot join
- Surgical intervention on the hand or wrist within the past 6 months
- Serious upper extremity injury or trauma within the past 6 months
- Diagnosis of carpal tunnel syndrome or peripheral nerve entrapment
- Numbness, paresthesia, or sensory impairment in the hand or wrist
- History of neurological disease (e.g., stroke, multiple sclerosis, peripheral neuropathy)
- Active pain, infection, open wound, or dermatological condition at the measurement site
- Reported hypersensitivity or intolerance to vibration
- Pregnancy
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Turkey (Türkiye)1 site
Acibadem Mehmet Ali Aydinlar University, Department of Physiotherapy and Rehabilitation
Istanbul
Ali Omer Acar, +905378262790, aliomer.acar@acibadem.edu.tr
Ali Omer Acar
About this study
Official title: Acute Effects of Smartphone-Delivered Local Vibration at Three Frequencies on Hand Grip Strength, Two-Point Discrimination, Pressure Pain Threshold, and Reaction Time in Healthy Young Adults: A Randomized Crossover Study
This study investigates the acute effects of smartphone-delivered local vibration on hand sensorimotor performance in healthy young adults. Using a custom-developed iPhone application, three vibration frequencies (80 Hz, 150 Hz, and 220 Hz) are applied to the dominant hand in a randomized crossover design with a minimum 48-hour washout between sessions.
The primary aim is to evaluate frequency-dependent dose-response effects on hand grip strength. Secondary aims include assessment of two-point discrimination (tactile spatial acuity), pressure pain threshold, and hand reaction time before and immediately after each vibration condition.
The study seeks to generate evidence on optimal application parameters for smartphone vibration as an accessible and portable local vibration source in clinical and educational settings.
Read the detailed description
BACKGROUND:
Local vibration (LV) has been investigated in physiotherapy and rehabilitation for modulating muscle activation, performance, and pain perception. Neurophysiological effects are mediated through tonic vibration reflex and enhanced sensory afferent input. LV offers a more targeted and portable approach compared to whole-body vibration (WBV). Short-duration LV applications have been shown to produce acute changes in muscle strength, tactile perception, reaction time, and pain threshold.
The hand region, with its high mechanoreceptor density and extensive cortical representation, provides a sensitive model for mechanical stimulation. Smartphones, through programmable haptic motors, can generate controlled vibration outputs and have been used in rehabilitation for vibrotactile feedback applications. However, studies combining assessment of grip strength, two-point discrimination, pressure pain threshold, and reaction time following mobile phone vibration on the hand are limited.
The frequency range (80-220 Hz) was selected to cover the optimal sensitivity band of Pacinian corpuscles (approximately 100-300 Hz), with 80 Hz being commonly used in LV literature. Three frequency levels (80, 150, 220 Hz) systematically represent the lower, middle, and upper portions of the range to explore a potential dose-response relationship.
STUDY DESIGN:
Randomized crossover design with three conditions (80 Hz, 150 Hz, 220 Hz). Each participant completes all three frequency conditions in separate sessions on different days. A minimum 48-hour washout period is maintained between sessions, and sessions are conducted at the same time of day. Application order is determined by counterbalanced randomization across the 6 possible sequences (3! = 6).
Measurement order (grip strength, PPT, 2PD, reaction time) is randomized for each participant at the first session and maintained consistently across all pre-tests, post-tests, and all three sessions. All measurements are performed by the same assessor. Post-vibration measurements are completed within 3-5 minutes. Total measurement time (excluding vibration) does not exceed 10 minutes per session.
VIBRATION PROTOCOL:
Vibration is delivered via a custom iPhone application using the device haptic motor. Each session applies one frequency condition. Stimulation consists of 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes).
Participant positioning: seated with back support, shoulder neutral, elbow approximately 90 degrees flexion, forearm supported on table in neutral position, wrist relaxed (0-20 degrees extension). The phone is held naturally in the dominant hand palm. Participants are instructed not to consciously squeeze or contract during application. Phone orientation and contact surface are kept consistent across repetitions and sessions.
OUTCOME MEASUREMENTS:
- Hand Grip Strength: Jamar hydraulic dynamometer with ASHT-recommended positioning. Three trials with 15-30 seconds rest between trials; mean of three trials used. Additional measurement taken if variation exceeds 10%.
- Pressure Pain Threshold (PPT): Pressure algometer on dominant hand thenar eminence, probe approximately 1 cm2, application rate approximately 1 kg/s. Three trials with 30 seconds rest; mean value used.
- Two-Point Discrimination (2PD): Baseline Two-Point Discriminator on dominant hand third finger distal pulp, eyes closed. Smallest distance correctly identified in at least 2 of 3 trials recorded as threshold (mm).
- Nelson Hand Reaction Time Test: Visual stimulus-motor response measured via ruler drop method. Three practice trials followed by 5 valid trials; best and worst values excluded, mean of remaining three used. Reaction time calculated using free-fall formula.
SAMPLE SIZE:
Based on Amiez et al. (2024), with conservatively reduced effect size (partial eta-squared approximately 0.10, Cohen f = 0.33), one-way repeated measures ANOVA power analysis (3 conditions, alpha = 0.05, power = 0.80, rho = 0.50) yielded a minimum of 18 completers. Target enrollment is 20 to account for potential dropouts.
STATISTICAL ANALYSIS:
Descriptive statistics. Primary analysis: two-way repeated measures ANOVA (3 frequencies x 2 time points) for each outcome variable. Post-hoc pairwise comparisons with Bonferroni correction. Effect sizes (partial eta-squared). Carry-over effects assessed. Non-parametric alternatives if assumptions are violated. Significance level: p less than 0.05.
- Conditions
- Healthy Volunteers, Vibration; Adverse Effect
- Being tested
- Smartphone Local Vibration at 80 Hz, Smartphone Local Vibration at 150 Hz, Smartphone Local Vibration at 220 Hz
- Keywords
- local vibration, smartphone vibration, haptic feedback, grip strength, two-point discrimination, pressure pain threshold, reaction time, sensorimotor performance, dose-response, crossover, hand function
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Smartphone Local Vibration at 80 HzDevice
Local vibration delivered via a custom-developed iPhone application using the device haptic motor at 80 Hz. Participant seated with back support, shoulder neutral, elbow 90 degrees flexion, forearm neutral on table support, wrist relaxed. Phone held naturally in dominant hand palm. Five repetitions of 45 seconds vibration + 15 seconds rest. Participants instructed not to consciously squeeze during application.
Smartphone Local Vibration at 150 HzDevice
Local vibration delivered via a custom-developed iPhone application using the device haptic motor at 150 Hz. Same positioning and protocol as 80 Hz condition. Five repetitions of 45 seconds vibration + 15 seconds rest.
Smartphone Local Vibration at 220 HzDevice
Local vibration delivered via a custom-developed iPhone application using the device haptic motor at 220 Hz. Same positioning and protocol as 80 Hz condition. Five repetitions of 45 seconds vibration + 15 seconds rest.
| Study group | Role | What they receive |
|---|---|---|
| 80 Hz Local Vibration | Experimental | Smartphone-delivered local vibration at 80 Hz applied to the dominant hand. Stimulation protocol: 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes). Represents the lower end of the tested frequency range. Receives: Device: Smartphone Local Vibration at 80 Hz |
| 150 Hz Local Vibration | Experimental | Smartphone-delivered local vibration at 150 Hz applied to the dominant hand. Stimulation protocol: 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes). Represents the middle of the tested frequency range. Receives: Device: Smartphone Local Vibration at 150 Hz |
| 220 Hz Local Vibration | Experimental | Smartphone-delivered local vibration at 220 Hz applied to the dominant hand. Stimulation protocol: 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes). Represents the upper end of the tested frequency range. Receives: Device: Smartphone Local Vibration at 220 Hz |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Hand Grip Strength
Hand grip strength measured with Jamar hydraulic dynamometer (kg) using ASHT-recommended positioning. Three trials per measurement; mean of three trials used. Pre-post difference assessed at each frequency condition (80 Hz, 150 Hz, 220 Hz).
Measured: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Secondary outcomes (3)
Change in Two-Point Discrimination (2PD)
Tactile spatial acuity measured with Baseline Two-Point Discriminator on dominant hand third finger distal pulp (mm). Smallest distance correctly identified in at least 2 of 3 trials recorded as threshold. Lower values indicate better tactile discrimination.
Measured: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Change in Pressure Pain Threshold (PPT)
Pressure pain threshold measured with pressure algometer on dominant hand thenar eminence (kg/cm2). Probe approximately 1 cm2, application rate approximately 1 kg/s. Mean of three trials used. Higher values indicate higher pain tolerance.
Measured: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Change in Hand Reaction Time
Visual stimulus-motor response time assessed with Nelson Hand Reaction Time Test (ms). Five valid trials after 3 practice trials; best and worst excluded, mean of remaining three used. Reaction time calculated via free-fall formula. Lower values indicate faster reaction.
Measured: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Apr 2026
- Study startApr 2026 (estimated)
- Primary completionJul 2026 (estimated)
- Study completionNov 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Healthy VolunteersStudies of the same condition, open and under way.
- More trials run by Acibadem 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
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- Randomized crossover with three conditions. Each participant receives all three vibration frequencies (80 Hz, 150 Hz, 220 Hz) in separate sessions on different days, with a minimum 48-hour washout between sessions. Application order is counterbalanced across the 6 possible sequences (3! = 6) using randomization.
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Acibadem University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ali Ömer Acar, Acibadem University
- Investigators
- Ali Omer Acar, Principal investigator, Acibadem Mehmet Ali Aydinlar University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07521228
- Sponsor's protocol ID
- ACU-FTR-AOA5
- Other IDs
- 2026-06/275
- Acronym
- SmartVib
- Status last verified
- Apr 2026
- First submitted
- 3 Apr 2026
- Last updated
- 9 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 9 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Acute Effects of Smartphone-Delivered Local Vibration at Three Frequencies on Hand Grip Strength, Two-Point Discrimination, Pressure Pain Threshold, and Reaction Time in Healthy Young Adults: A Randomized Crossover Study
- ClinicalTrials.gov ID
- NCT07521228
- Acronym / sponsor ID
- SmartVib / ACU-FTR-AOA5
- Conditions
- Healthy Volunteers, Vibration; Adverse Effect
- Keywords
- local vibration, smartphone vibration, haptic feedback, grip strength, two-point discrimination, pressure pain threshold, reaction time, sensorimotor performance
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- Acibadem UniversityUniversity, hospital or other
- Study start
- Apr 2026 (estimated)
- Primary completion
- Jul 2026 (estimated)
- Study completion
- Nov 2026 (estimated)
- First posted
- 9 Apr 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.
This study investigates the acute effects of smartphone-delivered local vibration on hand sensorimotor performance in healthy young adults. Using a custom-developed iPhone application, three vibration frequencies (80 Hz, 150 Hz, and 220 Hz) are applied to the dominant hand in a randomized crossover design with a minimum 48-hour washout between sessions.
The primary aim is to evaluate frequency-dependent dose-response effects on hand grip strength. Secondary aims include assessment of two-point discrimination (tactile spatial acuity), pressure pain threshold, and hand reaction time before and immediately after each vibration condition.
The study seeks to generate evidence on optimal application parameters for smartphone vibration as an accessible and portable local vibration source in clinical and educational settings.
Detailed description
BACKGROUND:
Local vibration (LV) has been investigated in physiotherapy and rehabilitation for modulating muscle activation, performance, and pain perception. Neurophysiological effects are mediated through tonic vibration reflex and enhanced sensory afferent input. LV offers a more targeted and portable approach compared to whole-body vibration (WBV). Short-duration LV applications have been shown to produce acute changes in muscle strength, tactile perception, reaction time, and pain threshold.
The hand region, with its high mechanoreceptor density and extensive cortical representation, provides a sensitive model for mechanical stimulation. Smartphones, through programmable haptic motors, can generate controlled vibration outputs and have been used in rehabilitation for vibrotactile feedback applications. However, studies combining assessment of grip strength, two-point discrimination, pressure pain threshold, and reaction time following mobile phone vibration on the hand are limited.
The frequency range (80-220 Hz) was selected to cover the optimal sensitivity band of Pacinian corpuscles (approximately 100-300 Hz), with 80 Hz being commonly used in LV literature. Three frequency levels (80, 150, 220 Hz) systematically represent the lower, middle, and upper portions of the range to explore a potential dose-response relationship.
STUDY DESIGN:
Randomized crossover design with three conditions (80 Hz, 150 Hz, 220 Hz). Each participant completes all three frequency conditions in separate sessions on different days. A minimum 48-hour washout period is maintained between sessions, and sessions are conducted at the same time of day. Application order is determined by counterbalanced randomization across the 6 possible sequences (3! = 6).
Measurement order (grip strength, PPT, 2PD, reaction time) is randomized for each participant at the first session and maintained consistently across all pre-tests, post-tests, and all three sessions. All measurements are performed by the same assessor. Post-vibration measurements are completed within 3-5 minutes. Total measurement time (excluding vibration) does not exceed 10 minutes per session.
VIBRATION PROTOCOL:
Vibration is delivered via a custom iPhone application using the device haptic motor. Each session applies one frequency condition. Stimulation consists of 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes).
Participant positioning: seated with back support, shoulder neutral, elbow approximately 90 degrees flexion, forearm supported on table in neutral position, wrist relaxed (0-20 degrees extension). The phone is held naturally in the dominant hand palm. Participants are instructed not to consciously squeeze or contract during application. Phone orientation and contact surface are kept consistent across repetitions and sessions.
OUTCOME MEASUREMENTS:
- Hand Grip Strength: Jamar hydraulic dynamometer with ASHT-recommended positioning. Three trials with 15-30 seconds rest between trials; mean of three trials used. Additional measurement taken if variation exceeds 10%.
- Pressure Pain Threshold (PPT): Pressure algometer on dominant hand thenar eminence, probe approximately 1 cm2, application rate approximately 1 kg/s. Three trials with 30 seconds rest; mean value used.
- Two-Point Discrimination (2PD): Baseline Two-Point Discriminator on dominant hand third finger distal pulp, eyes closed. Smallest distance correctly identified in at least 2 of 3 trials recorded as threshold (mm).
- Nelson Hand Reaction Time Test: Visual stimulus-motor response measured via ruler drop method. Three practice trials followed by 5 valid trials; best and worst values excluded, mean of remaining three used. Reaction time calculated using free-fall formula.
SAMPLE SIZE:
Based on Amiez et al. (2024), with conservatively reduced effect size (partial eta-squared approximately 0.10, Cohen f = 0.33), one-way repeated measures ANOVA power analysis (3 conditions, alpha = 0.05, power = 0.80, rho = 0.50) yielded a minimum of 18 completers. Target enrollment is 20 to account for potential dropouts.
STATISTICAL ANALYSIS:
Descriptive statistics. Primary analysis: two-way repeated measures ANOVA (3 frequencies x 2 time points) for each outcome variable. Post-hoc pairwise comparisons with Bonferroni correction. Effect sizes (partial eta-squared). Carry-over effects assessed. Non-parametric alternatives if assumptions are violated. Significance level: p less than 0.05.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Randomized crossover with three conditions. Each participant receives all three vibration frequencies (80 Hz, 150 Hz, 220 Hz) in separate sessions on different days, with a minimum 48-hour washout between sessions. Application order is counterbalanced across the 6 possible sequences (3! = 6) using randomization.
| Arm | Type | Receives |
|---|---|---|
| 80 Hz Local Vibration | Experimental | Device: Smartphone Local Vibration at 80 HzSmartphone-delivered local vibration at 80 Hz applied to the dominant hand. Stimulation protocol: 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes). Represents the lower end of the tested frequency range. |
| 150 Hz Local Vibration | Experimental | Device: Smartphone Local Vibration at 150 HzSmartphone-delivered local vibration at 150 Hz applied to the dominant hand. Stimulation protocol: 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes). Represents the middle of the tested frequency range. |
| 220 Hz Local Vibration | Experimental | Device: Smartphone Local Vibration at 220 HzSmartphone-delivered local vibration at 220 Hz applied to the dominant hand. Stimulation protocol: 5 repetitions of 45 seconds vibration + 15 seconds rest (total approximately 5 minutes). Represents the upper end of the tested frequency range. |
Who may qualify
- Ages
- 18 to 25 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Healthy university students aged 18-25 years
- Willing to participate and provide written informed consent
- Able to attend three separate measurement sessions
Key exclusion criteria (8 listed)
- Surgical intervention on the hand or wrist within the past 6 months
- Serious upper extremity injury or trauma within the past 6 months
- Diagnosis of carpal tunnel syndrome or peripheral nerve entrapment
- Numbness, paresthesia, or sensory impairment in the hand or wrist
- History of neurological disease (e.g., stroke, multiple sclerosis, peripheral neuropathy)
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 |
|---|---|---|
| Smartphone Local Vibration at 80 HzLocal vibration delivered via a custom-developed iPhone application using the device haptic motor at 80 Hz. Participant seated with back support, shoulder neutral, elbow 90 degrees flexion, forearm neutral on table support, wrist relaxed. Phone held naturally in dominant hand palm. Five repetitions of 45 seconds vibration + 15 seconds rest. Participants instructed not to consciously squeeze during application. | Device | 80 Hz Local Vibration |
| Smartphone Local Vibration at 150 HzLocal vibration delivered via a custom-developed iPhone application using the device haptic motor at 150 Hz. Same positioning and protocol as 80 Hz condition. Five repetitions of 45 seconds vibration + 15 seconds rest. | Device | 150 Hz Local Vibration |
| Smartphone Local Vibration at 220 HzLocal vibration delivered via a custom-developed iPhone application using the device haptic motor at 220 Hz. Same positioning and protocol as 80 Hz condition. Five repetitions of 45 seconds vibration + 15 seconds rest. | Device | 220 Hz Local Vibration |
Primary outcome
Change in Hand Grip Strength
Time frame: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Hand grip strength measured with Jamar hydraulic dynamometer (kg) using ASHT-recommended positioning. Three trials per measurement; mean of three trials used. Pre-post difference assessed at each frequency condition (80 Hz, 150 Hz, 220 Hz).
3 secondary outcomes
Change in Two-Point Discrimination (2PD)
Time frame: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Change in Pressure Pain Threshold (PPT)
Time frame: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Change in Hand Reaction Time
Time frame: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Apr 2026.
- Individual participant dataSharing planned: Undecided
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Screening Protocol
Pain
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.
Ali Omer Acar principal investigator
Acibadem Mehmet Ali Aydinlar University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Smartphone Local Vibration at 80 Hz, Smartphone Local Vibration at 150 Hz and Smartphone Local Vibration at 220 Hz in people with Healthy Volunteers and Vibration; Adverse Effect, run by Acibadem 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 8 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: opening soon, as of the sponsor's last update on 9 Apr 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ali Omer Acar (+905378262790, aliomer.acar@acibadem.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Hand Grip Strength (time frame: Immediately before and immediately after vibration application at each session (3 sessions, minimum 48 hours apart)). 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 9 Apr 2026.