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Stabilometric and Baropodometric Evaluation After Osteopathic Scaphoid Tug Manipulation

Stabilometric and Baropodometric Evaluation of Osteopathic Scaphoid Tug Manipulation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05583760
Enrollment
36
Registered
2022-10-18
Start date
2022-10-18
Completion date
2023-02-07
Last updated
2023-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Manipulation, Osteopathic

Brief summary

This is a clinical, longitudinal, prospective and randomised study in which the subject will be assessed by stabilometric and baropodometric techniques on two occasions (before being subjected to the scaphoid tug manipulation for the experimental group or placebo technique in the case of the control group).

Interventions

PROCEDUREExperimental: Osteopathic manipulation TUG for scaphoid bone

The sequence of execution of the scaphoid TUG technique shall be applied as follows. Patient in the supine position. The inner hand of the intervener makes contact with the pisiform through the hypothenar eminence and ulnar border of the hand over the scaphoid tubercle, the outer hand reinforces the contact. The thumbs are directed to the sole of the patient's foot. The parameters are sought by bringing the sole of the foot into eversion, thus bringing the scaphoid into internal rotation (the direction of correction). In order to reduce the slack, the operator drops his body weight backwards while increasing the internal rotation parameter of the scaphoid. The manipulation is performed by associating a rapid traction movement with an increase of the correction parameter towards the internal rotation of the scaphoid.

PROCEDURESham group: Sham osteopathic manipulation TUG for scaphoid bone

The intervention will be performed in the same way as the intervention group, without actually performing the TUG manipulation on the scaphoid bone, only placing it in tension.

Sponsors

Cardenal Herrera University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

SINGLE BLIND (PARTICIPANT)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Subjects with right scaphoid external rotation dysfunction

Exclusion criteria

* Suffering from disorders that alter balance (tension headaches, vertigo, migraines...). * Deformities, orthopaedic injuries or sequelae in the limbs or spine that may alter postural statics (valgus-varus, lower limb operations, lower limb dysmetries, scoliosis, etc.). * Pathologies or sequelae related to the postural sensors or disorders in the same: * Uncorrected visual defects. * Vestibular disorders. * Uncorrected stomatological disorders. * Sensory alterations in the foot sensor (Hypoaesthesia, Morton's neuroma, tarsal canal syndrome, etc.). * Cutaneous alterations that influence the foot pick-up (papillomas, plantar warts, ingrown toenails, etc.). * Ingestion of medication that alters the perception of stability. * Having any contraindication to the scaphoid tug technique. * Having carried out intense physical activity immediately prior to the study. * Having received osteopathic treatment in the last month.

Design outcomes

Primary

MeasureTime frameDescription
stabilometric measurements: oscillation about the X-axisfive minutes post-intervention(mm)
stabilometric measurements: oscillation about the Y-axisfive minutes post-intervention(mm)
stabilometric measurements: area of the ellipsefive minutes post-intervention(cm2)
static baropodometric measurements: scan Foot bearing areafive minutes post-intervention(cm2)
static baropodometric measurements: scan percentage of body load supported by each footfive minutes post-intervention
static baropodometric measurements: scan point of maximum plantar pressurefive minutes post-intervention(kg/cm2)

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026