ClinicalTrials.gg
RecruitingNCT07832994Updated Sep 22, 2026

Metaboic Syndrome and Fatty Liver in Celiac Disease Females: Reponse to Exercise in Adolescents

An interventional study of walking exercise in Celiac Disease, Metabolic Syndrome and Non Alcoholic Fatty Liver, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to female participants aged 13 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-09-22.

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

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
13 Years to 17 Years
Sex
Female
01

Study summary

metabolic syndrome and fatty liver is common in adolescents with celiac diseases. exercise may control these cardiovascular risk factors

Read the detailed description

forty metabolic syndrome and fatty liver female adolescents with celiac diseases will assigned to exercise group or control group. the group will contain twenty patients. control group will be wait list. exercise group will perform 40 minutes of walking on a treadmill three times weekly for three months.

02

Conditions studied

  • Celiac Disease
  • Metabolic Syndrome
  • Non Alcoholic Fatty Liver
03

In context

Celiac Disease

352 studies on the registry are indexed under Celiac Disease; 77 are open to participants now.

This study's planned enrollment of 40 is below the median of 50 across 214 interventional studies indexed under Celiac Disease.

Browse Celiac Disease studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

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

04

Who can participate

Ages eligible
13 Years to 17 Years
Sexes eligible
Female
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

  • celiac disease
  • metabolic syndrome
  • nonalcholic fatty liver

Exclusion criteria

Exclusion Criteria:

  • cardiac disease
  • renal failure
  • respiratory disease
05

Study design

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

Study arms

  • Experimental
    group I

    twenty metabolic syndrome and fatty liver female adolescents with celiac diseases will will perform 40 minutes of walking on a treadmill three times weekly for three months.

    Behavioral: walking exercise

  • No intervention
    group II

    twenty metabolic syndrome and fatty liver female adolescents with celiac diseases will be wait list for three months.

Interventions

  • Behavioralwalking exercise

    twenty metabolic syndrome and fatty liver female adolescents with celiac diseases will will perform 40 minutes of walking on a treadmill three times weekly for three months.

06

What researchers measure

Primary outcomes

  1. alanine transamianse

    It will be asssessed in plasma

    Time frame: It will be measured after 12 weeks

Secondary outcomes

  1. Asparate tranamianse

    it will be assessed in plasma

    Time frame: It will be measured after 12 weeks

  2. gamma glutamyl transferase

    it will be assessed in plasma

    Time frame: it will be measured after 12 weeks

  3. alkaline phosphatase

    it will be assessed in plasma

    Time frame: it will be measured after 12 weeks

  4. Body mass index

    it wil be measured with empty stomach and bladder

    Time frame: it will be assessed after 12 weeks

  5. wasit circumference

    it will be assessed at the level of umbilicus

    Time frame: it will be assessed after 12 weeks

  6. systolic blood pressure

    it will be assessed at level of brachial artery

    Time frame: it will be assessed after 12 weeks

  7. diastolic blood pressure

    it will be assessed at level of brachial artery

    Time frame: it will be assessed after 12 weeks

  8. blood glucose

    it will be measured in fasting status in blood

    Time frame: it will be assessed after 12 weeks

  9. high density lipoproteins

    it will be assessed in plasma

    Time frame: it will be assessed after 12 weeks

  10. triglycerides

    it will be assessed in plasma

    Time frame: it will be assessed after 12 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Dec 2026, 4 months after the start.

Of 82 non-industry interventional studies with no phase under Celiac Disease, half reached primary completion within 28 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 60. This study's planned 4 months is below that.

Counting every sponsor, half of 87 studies reached it within 27 months; a quarter within 12 and three quarters within 56.

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

Registered
Sep 16, 2026
First posted
Sep 22, 2026
StartActual
Aug 15, 2026
Primary completionEst.
Dec 15, 2026
CompletionEst.
Dec 15, 2026
Last update
Sep 22, 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 Sep 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07832994
Lead sponsor
Cairo University
Responsible party
Ali Mohamed Ali ismail (lecturer of physical therapy for Cardiovascular, Respiratory disorder and Geriatrics, Faculty of Physical Therapy, Cairo University, Cairo University) — Principal investigator
First posted
Sep 22, 2026
Start date
Aug 15, 2026
Primary completion
Dec 15, 2026 (estimated)
Completion
Dec 15, 2026 (estimated)
Last update
Sep 22, 2026

Study contacts

Ali MA Ismail, PhD
Contact
ali.mohamed@pt.cu.edu.eg
+201005154209
Fatma mohamed, PhD
Contact
fatmaraed1994@gmail.com
+201033321109
Ali MA Ismail, PHD
principal investigator · Cairo University

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion