Bone Myoregulation Reflex and Postural Control in Vitamin D Deficiency

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-40
SponsorIstanbul Physical Medicine Rehabilitation Training and Research Hospital

About this trial

This observational study aims to investigate the relationship between vitamin D deficiency, postural stability, and neuromuscular control mechanisms in adults. The study will compare individuals with vitamin D deficiency and healthy controls.

Participants will undergo a single-session evaluation including surface electromyography and postural stability assessments during standing tasks under different loading and vibration conditions. No invasive procedures, medications, or blood sampling will be performed. Previously obtained routine laboratory results will be used for vitamin D status.

The study is designed to improve understanding of neuromuscular responses associated with vitamin D deficiency and to contribute to future rehabilitation strategies.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age 20 to 40 years.

Ability to provide written informed consent.

Vitamin D deficiency group: serum 25-hydroxyvitamin D level <10 ng/mL measured within the last 3 months (routine clinical testing).

Healthy control group: normal vitamin D status based on routine clinical testing within the last 3 months.

Disqualifiers

Known metabolic bone disease other than vitamin D deficiency.

Neurological disorder (central or peripheral) or neuromuscular disease.

History of lower-limb surgery, fracture, or prosthesis affecting standing balance.

Vestibular disorder.

Trial population

Adults aged 20 to 40 years recruited from the outpatient clinics of Istanbul Physical Medicine and Rehabilitation Training and Research Hospital. Participants will include individuals with laboratory-confirmed vitamin D deficiency and healthy volunteers with normal vitamin D status.

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

24 Participants
are grouped into 2 trial groups
Group A: Vitamin D Deficiency Group
Group B: Healthy Control Group

Trial outcomes

Primary outcomes

1

Postural Stability Parameters

Postural stability parameters measured during single-leg and double-leg standing using force platform and surface electromyography, including postural sway and neuromuscular response variables.

Time frame
Single assessment session (baseline)

Secondary outcomes

1

Neuromuscular Reflex and Muscle Activation Patterns

Surface electromyography-derived muscle activation and reflex modulation parameters recorded under different loading and vibration conditions.

Time frame
Single assessment session (baseline)
2

Effect of Loading and Vibration on Postural Control

Changes in postural stability and neuromuscular responses under loaded and unloaded conditions with and without vibration.

Time frame
Single assessment session (baseline)

Other outcomes

Sponsors and contacts

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