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Flat FeetNCT07140861

Effect of Core Stability Exercises in Individuals With Bilateral Flexible Flat Foot

A study testing Conventional and Experimental in people with Flat Feet, run by Cairo University at 2 sites in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

There is a gap of literature about the role of core stability exercises on management of flexible flatfoot, as a result this study will take a deeper look on the effect of core stability exercises on navicular height, Arch height index, balance and disability function of ankle joint in individuals with bilateral… Read more about this study

Who is it for?
Ages 18 to 40 years
Conditions the study is for
Flat Feet
What is being tested?
Conventional and Experimental
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
2 sitesEgypt
Study dates
1 Sep 2025to 1 May 2026
Phase
Interventional
Are there results?
None posted in the registry

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 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 40 Participants of both genders with bilateral flexible flatfoot.
  • Their age ranges from 18 to 39 years.
  • All Participants with a navicular drop (ND) greater than 10 mm.
  • Body mass index from 18.5-25 kg/m2

Who cannot join

  • Traumatic condition of the lower limbs.
  • History of Fracture of the lower limbs.
  • previous orthopedic disorders or neurologic deficit of the lower limbs.
  • Previous surgery of the lower limbs.
  • Any sensory problems.
  • Leg length discrepancy.
Show all 10Show fewer
  • Neuromuscular disease like multiple scelerosis.
  • Unilateral flexible flat foot.
  • Rigid flat foot.
  • Any lumbar spine problems

Trial locations and contacts

2 sites in 1 country.

Egypt2 sites
  • Physical therapy College - Cairo university

    Cairo

  • Physical Therapy faculty, Cairo University

    Cairo

Other trials in Egypt

About this study

Official title: Effect of Core Stability Exercises on Medial Longitudinal Arch Height and Balance in Individuals With Bilateral Flexible Flat Foot

There is a gap of literature about the role of core stability exercises on management of flexible flatfoot, as a result this study will take a deeper look on the effect of core stability exercises on navicular height, Arch height index, balance and disability function of ankle joint in individuals with bilateral flexible flat foot.

Read the detailed description

It was proved that Individuals with flexible flat foot have reduced core stability. Thus, core stability must be assessed while treating individuals with flexible flat foot and interventions that address core stability must be included in the treatment of flexible flat foot . It was demonstrated that there was a poorer balance in individual with bilateral flexible flat foot. Therefore, it is recommended to add balance training exercises to traditional physical therapy program in cases of flatfoot patients .

40 Participants of both genders with bilateral flexible flatfoot. will be assigned randomly into 2 equal groups: Group A (control group): will receive conventional therapy. Group B (Experimental group): will receive core training protocol and conventional therapy. Subjects will receive 3 sessions per week for 6 weeks.

Outcome measures:

  1. Navicular height: will be evaluated by navicular drop test.
  2. Medial longitudinal arch height: will be evaluated by Arch height index (AHI).
  3. Balance: will be evaluated by Biodex Balance System.
  4. Disability function of ankle joint: will be evaluated by Arabic version of foot function index scale.
Conditions
Flat Feet
Being tested
Conventional, Experimental
Keywords
core stability exercises, medial longitudinal arch height, balance, bilateral flexible flat foot
Medical subject headings
Flatfoot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ConventionalOther

    patients will receive conventional therapy that include

    1. Short foot exercises
    2. Towel-curl exercise
    3. Heel raise exercise
    4. Calf stretch
  • ExperimentalOther

    Core stability exercises:

    The training programs will last 6 weeks and comprise 3 training sessions per week. Each training session lasted 30 min, starting with a brief, standardized warm-up program mainly consisting of low-intensity core strength exercises to prepare the neuromuscular system for the training loads and ending with a cool-down program (i.e., dynamic stretching). During the main part of training, research group will conduct the "big 3" exercises as described by McGill (Mcgill, 2001). These include the curl-up, side bridge, and quadruped position. In other words, every single training session consisted of frontal, dorsal, and lateral core exercises. Training intensity will be progressed and individually increased over the 6-week training program by modulating lever lengths, movement velocity

Study groups in NCT07140861
Study groupRoleWhat they receive
Control groupActive comparatorControl group will receive conventional treatment
Receives: Other: Conventional
Study groupExperimentalStudy group: will receive core training protocol and conventional therapy.
Receives: Other: Conventional; Other: Experimental

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Navicular height

    Measured: at enrollment and at the end of 6 weeks of treatment

  2. Balance

    Dynamic balance will be assessed by Biodex system

    Measured: at enrollment and at the end of 6 weeks of treatment

Secondary outcomes (2)
  1. Medial longitudinal arch height

    Measured: at enrollment and at the end of 6 weeks of treatment

  2. Function of ankle joint

    Function of ankle joint will be assessed by Arabic version of foot function index scale.

    Measured: at enrollment and at the end of 6 weeks of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Aug 2025
  2. Study start1 Sep 2025
  3. Primary completion1 Apr 2026
  4. Study completion1 May 2026

Resources

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07140861
Sponsor's protocol ID
Physical Therapy 52043
Status last verified
Jul 2026
First submitted
23 Jul 2025
Last updated
14 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Conventional and Experimental in people with Flat Feet, run by Cairo University at 2 sites in Egypt.

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 4 inclusion and 10 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: finished, as of the sponsor's last update on 14 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Egypt. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Navicular height (time frame: at enrollment and at the end of 6 weeks of treatment). The study lists 2 primary outcomes in all. 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 14 Jul 2026.

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