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CompletedNCT06988631Updated May 25, 2025

Sensorimotor Organization in Individuals With General Joint Hypermobility

An interventional study of Sensory treatment and foot care booklet in Generalized Joint Hypermobility, sponsored by Gazi University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 25 Years. Per ClinicalTrials.gov, last updated 2025-05-25.

Sponsored by Gazi University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Jan 2024, registered May 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
65
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
All
01

Study summary

This study is the first to examine the effect of sole sensory training on sensorimotor organization in individuals with GEH. Individuals with a Beighton score of 5 and above were included in the study. Within the scope of the study, individuals with general joint hypermobility (GEH) were divided into intervention and control groups by the Randomization method. The intervention group received sole sensory training in the home environment. Both groups were given a foot care brochure. The individuals' sole sensory and balance skills were evaluated before and after the intervention. As a result of the study, the intervention aimed to prevent injuries and disabilities that may occur due to joint laxity by improving sole sensory and balance.

02

Conditions studied

  • Generalized Joint Hypermobility

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Keywords

  • joint hypermobility
  • food sense
  • Sensorimotor
03

In context

Joint Instability

115 studies on the registry are indexed under Joint Instability; 21 are open to participants now.

This study's enrollment of 65 is above the median of 46 across 58 interventional studies indexed under Joint Instability.

Browse Joint Instability studies →

Lead sponsor

Gazi University is the lead sponsor of 551 studies on the registry; 102 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Persons with a Beighton score ≥5 without any systemic disease
  • Asymptomatic persons

Exclusion criteria

Exclusion Criteria:

  • People who have had an upper or lower extremity injury in the last 3 months,
  • People who have a history of fractures or surgery in the last year,
  • People who have been pregnant in the last year,
  • Those diagnosed with Ehlers-Danlos Syndrome (EDS), hypermobile Ehlers-Danlos syndrome (hEDS), or hypermobility spectrum disorders (HSD)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
65 participants (actual)

Study arms

  • Active comparator
    Kontrol group

    Participants were given brochures and training on foot care and health.

    Other: foot care booklet

  • Experimental
    exercise group

    Participants were asked to practice the foot sole sensory training program at home every day for 2 weeks.

    Other: Sensory treatment

Interventions

  • OtherSensory treatment

    Participants were asked to practice the foot sole sensory training program at home every day for 2 weeks.

  • Otherfoot care booklet

    Participants were given a booklet about healthy feet and were informed.

06

What researchers measure

Primary outcomes

  1. Light touch sensation

    It was evaluated using the Semmes-Weinstein Monofilament (SWM) test kit.

    Time frame: 2 weeks

  2. Two-Point Separation sensation

    A discriminator was used to assess two-point discrimination perception.

    Time frame: 2 weeks

  3. Vibration sense

    A 128 Hz tuning fork was used to evaluate vibration sensation.

    Time frame: 2 weeks

Secondary outcomes

  1. Proprioception

    Joint position sense test for proprioception assessment was performed using a digital goniometer device.

    Time frame: 2 weeks

  2. Muscle Strength

    A hand-held dynamometer (Lafayette Instrument®, Layafette, IN) was used to determine muscle strength for both lower extremities of the individuals.

    Time frame: 2 weeks

  3. Balance

    Dynamic balance of individuals was assessed with the Y Balance Test.

    Time frame: 2 weeks

07

Study locations

1 site
  • Erzurum technical university
    Erzurum, State/Province 25200, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06988631
Lead sponsor
Gazi University
Responsible party
Ayse Simsek (Principal Investigator, Gazi University) — Principal investigator
First posted
May 25, 2025
Start date
Jan 15, 2024
Primary completion
Nov 15, 2024
Completion
Dec 15, 2024
Last update
May 25, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2025. You cannot join it, but the record below documents what was studied.

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