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Subclinical hypothyroïdismNCT07599241

Additive Efficacy of Physical Activity Program in Hypthyroidism Elder Females With Glaucoma and Fatty Liver Issues

A study testing physical activity in people with Subclinical hypothyroïdism and Non-Alcoholic Fatty Liver Disease, run by Cairo University at 1 site in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

additive efficacy of physical activity program in hypthyroidism in elder females with glaucoma and fatty liver issues was not investigated Read more about this study

Who is it for?
Ages 65 to 75 years, women only
What is being tested?
physical activity
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteEgypt
Study dates
15 Mar 2026to 15 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 65 to 75 years
  • Women only
  • No healthy volunteers
  • Older adult

Who may be able to join

  • subclinical hypothrodism (significant form)
  • primary opened angle gaulcoma in both eyes with ocular hypertension in both eyes )(high-tension typed glaucoma)
  • fatty liver (non alcholic type)
  • elder females

Who cannot join

  • respiratory issues
  • cardiac issues
  • renal issues

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ali MA Ismail, lecturer contact

01005154209

ali.mohamed@pt.cu.edu.eg

Egypt1 site, 1 recruiting
  • Cairo University

    Dokki, Giza Governorate, 11432

    ali AM Ismail, lecturer, +201005154209, ali.mohamed@pt.cu.edu.eg

    Recruiting

Other trials in Egypt

About this study

additive efficacy of physical activity program in hypthyroidism in elder females with glaucoma and fatty liver issues was not investigated

Read the detailed description

hypthyroidism elder females (n=40) with glaucoma and fatty liver issues will randomly divided into group number 1 (n=20) that will recive their levothyroxine and physical activity program on treadmill thrice weehly for 6 month or group number II (n=20) that will receive levothyroxine only

Being tested
physical activity, usual care
Medical subject headings
Non-alcoholic Fatty Liver Disease, Glaucoma, Open-Angle

What participants receive

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

  • physical activityBehavioural

    hypthyroidism elder females (n=20) with glaucoma and fatty liver issues that will recive their levothyroxine and physical activity program on treadmill thrice weehly for 6 month

  • usual careOther

    hypthyroidism elder females (n=20) with glaucoma and fatty liver issues that will recive their levothyroxine only

Study groups in NCT07599241
Study groupRoleWhat they receive
group number 1Experimentalhypthyroidism elder females (n=20) with glaucoma and fatty liver issues recive their levothyroxine and physical activity program on treadmill thrice weekly for 6 month
Receives: Behavioral: physical activity
group number 2Active comparatorhypthyroidism elder females (n=20) with glaucoma and fatty liver issues will recive their levothyroxine only
Receives: Other: usual care

What is being measured

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

  1. intraocular pressure

    it will be assessed in both eyes

    Measured: 6 months

Secondary outcomes (13)
  1. body mass index

    it will be assessed on empty stomach and bladder

    Measured: 6 months

  2. waist circumfrence

    it will be assessed by tape at umblical level

    Measured: 6 months

  3. systolic blood pressure

    it will be assessed by sphygmomanmometer

    Measured: 6 months

  4. diastolic blood pressure

    it will be assessed by sphygmomanmometer

    Measured: 6 months

  5. glaucoma assocaited life quality survey

    it is a questionaire evaluates life quality

    Measured: 6 months

  6. triglyceridss

    it will be assessed in serum

    Measured: 6 months

  7. high density lipoproteines

    it will be assesed in serum

    Measured: 6 months

  8. alanine transamianses

    it will be assessed in serum

    Measured: 6 months

  9. aspartate trasnamiansses

    it will be assessed in serum

    Measured: 6 months

  10. physical conclusion of short form survey

    it will assess physical quality of lifes of females

    Measured: 6 months

  11. Mental conclusion of short form survey

    it will assess physical quality of lifes of females

    Measured: 6 months

  12. thyroid stimualting horomone

    it will be assessed in serum

    Measured: 6 months

  13. fasting glycemia value

    it will be assessed in serum

    Measured: 6 months

Timeline

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

  1. First posted20 May 2026
  2. Study start15 Mar 2026
  3. Primary completion15 Dec 2026 (estimated)
  4. Study completion15 Dec 2026 (estimated)

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
Single blind
Who is masked
Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07599241
Sponsor's protocol ID
IRB000-14233-75
Status last verified
May 2026
First submitted
9 May 2026
Last updated
20 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing physical activity in people with Subclinical hypothyroïdism and Non-Alcoholic Fatty Liver Disease, run by Cairo University at 1 site 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 3 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: looking for participants now, as of the sponsor's last update on 20 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Ali MA Ismail, lecturer (01005154209, ali.mohamed@pt.cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

intraocular pressure (time frame: 6 months). 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 20 May 2026.

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