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Active, not recruitingNCT07761000Updated Aug 12, 2026

Evaluation of Spinal Posture, Balance, and Core Muscle Endurance in Individuals With Plantar Fasciitis

An observational study in Plantar Fasciitis of Both Feet, sponsored by Ahi Evran University Education and Research Hospital. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by Ahi Evran University Education and Research Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
64
Ages
18 Years to 50 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 42 studies in Fasciitis, Plantar with a site in Turkey — 15 open to participants now, 16 under way, none of them phase 3. Fasciitis, Plantar · Turkey.

Planned enrollment
8th of 14
64 · median 77
Started
2026
with 8 others
Observational
14 of 42
5 open now
Primary completion
2026-12
later than 9 of 15 live
Registered
37th of 42
by date
Lead sponsor
2 of 42
Ahi Evran University Education and Research Hospital

Among the 42 studies in Fasciitis, Plantar with a site in Turkey, this one is the 8th largest by planned enrollment of the 14 observational ones that give a count, is one of 9 that started in 2026, is one of 14 observational ones, reaches primary completion later than 9 of the 15 other live ones, and was the 37th registered.

Fasciitis, Plantar

223 studies on the registry are indexed under Fasciitis, Plantar; 58 are open to participants now.

This study's planned enrollment of 64 is close to the median of 60 across 24 observational studies indexed under Fasciitis, Plantar.

Browse Fasciitis, Plantar studies →

Open to participants now

15 of the 42 studies in Fasciitis, Plantar with a site in Turkey are open now, in 1 country. Each count lists the studies.

All 15 open studies →

Where they have run

Who these studies take

Of the 29 Fasciitis, Plantar studies recruiting now, 5 (17%) set no upper age limit and 21 (72%) stop at 75 or younger; 0 take children under 18; 4 take healthy volunteers.

This study: 18 Years to 50 Years · all sexes · healthy volunteers too.

The full table on the hub →
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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 42 studies in Fasciitis, Plantar with a site in Turkey, or all of them as a file.
02

Study summary

The study will include individuals aged 18-50 years who present to the Physical Medicine and Rehabilitation Outpatient Clinic of Kırşehir Ahi Evran University Hospital with heel pain and are diagnosed with plantar fasciitis. The control group will consist of healthy volunteers within the same age range who do not have heel pain and are recruited from among patients' relatives. Individuals with any orthopedic deformity or neurological disorder will be excluded from both groups.

Read the detailed description

The study will include individuals aged 18-50 years who present to the Physical Medicine and Rehabilitation Outpatient Clinic of Kırşehir Ahi Evran University Hospital with heel pain and are diagnosed with plantar fasciitis. The control group will consist of healthy volunteers within the same age range who do not have heel pain and are recruited from among patients' relatives. Individuals with any orthopedic deformity or neurological disorder will be excluded from both groups.

Core muscle endurance will be assessed using the McGill Core Endurance Tests, dynamic balance using the Y-Balance Test, and static balance using the Single-Leg Stance Test. Foot function will be evaluated using the Foot Function Index, spinal posture using a bubble inclinometer, and pain intensity using the Visual Analog Scale.

03

Conditions studied

  • Plantar Fasciitis of Both Feet

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Keywords

  • Plantar fasciitis
  • spinal posture
  • static balance
  • dynamic balance
  • foot function
  • heel pain
04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will consist of individuals aged 18-50 years. The case group will include patients who present to the Physical Medicine and Rehabilitation Outpatient Clinic of Kırşehir Ahi Evran University Hospital with heel pain and are diagnosed with plantar fasciitis. The control group will consist of healthy volunteers recruited from among patients' relatives who are within the same age range and have no heel pain. Individuals with an orthopedic deformity or neurological disorder that may affect posture, balance, or physical performance will not be included in the study.

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

  1. Being between 18-50 years of age,
  2. Having heel pain for at least 3 months,
  3. Having a clinical diagnosis of plantar fasciitis.

Exclusion criteria

Exclusion Criteria:

  1. Presence of neurological disease
  2. Vestibular disorder
  3. Rheumatological disease
  4. History of lower extremity surgery
  5. Vision problem that may affect balance.
  6. Pregnancy
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
64 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • Plantar fasciitis

    evaluation

    Other: evaluation

  • Healthy

    evaluation

    Other: evaluation

Interventions

  • Otherevaluation

    All participants will undergo a standardized evaluation. Core muscle endurance will be assessed using the McGill Core Endurance Tests. Dynamic balance will be evaluated using the Y-Balance Test, while static balance will be assessed using the Single-Leg Stance Test. Spinal posture will be evaluated using a bubble inclinometer. Foot function will be assessed using the Foot Function Index, and heel pain intensity will be measured using the Visual Analog Scale. No therapeutic intervention will be administered as part of the study.

06

What researchers measure

Primary outcomes

  1. Spinal Posture Assessed Using a Bubble Inclinometer

    Sagittal spinal posture will be evaluated using a bubble inclinometer. Thoracic kyphosis and lumbar lordosis angles will be measured in degrees under standardized standing conditions. Higher angular values indicate a greater degree of the corresponding spinal curvature.

    Time frame: During the single assessment session, approximately 10 minutes.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — privacy of personal information

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Aug 2026 (actual). Primary completion is estimated for Dec 2026, 3 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 4, 2026
First posted
Aug 12, 2026
StartActual
Aug 5, 2026
Primary completionEst.
Dec 1, 2026
CompletionEst.
Jan 15, 2027
Last update
Aug 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07761000
Lead sponsor
Ahi Evran University Education and Research Hospital
Responsible party
Esra BAYRAMOĞLU DEMİRDÖĞEN (Lecturer, Ahi Evran University Education and Research Hospital) — Principal investigator
First posted
Aug 12, 2026
Start date
Aug 5, 2026
Primary completion
Dec 1, 2026 (estimated)
Completion
Jan 15, 2027 (estimated)
Last update
Aug 12, 2026

Study contacts

Esra BAYRAMOĞLU DEMİRDÖĞEN
principal investigator · Kırşehir Eğitim ve Araştırma Hastanesi

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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