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Insulin Resistance-abdominal Fats -Post Menopausal WomenDry needleNCT07365878

Effect of Dry Needling on Insulin Resistance in Obese Post Menopausal Women

A study testing Dry Needle in people with Insulin Resistance-abdominal Fats -Post Menopausal Women, run by Cairo University at 1 site 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

The aim of the study is to determine the effect Dry Needling of on insulin resistance in obese postmenopausal women. Read more about this study

Who is it for?
Ages 48 to 60 years
What is being tested?
Dry Needle
Could I receive a placebo?
No, everyone receives an active treatment
How many people
52 participants
Where
1 siteEgypt
Study dates
1 Jan 2025to 1 Dec 2025
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 48 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • • All participants post-menopausal from at least 3 years.
  • All participants' ages will be ranged from 48-60 years old.
  • All participants BMI will exceed 25-30 kg/m2.
  • All participants waist hip ratio will be equal or more than 0, 90.

Who cannot join

  • • Surgical liposuction within the last 12 months.
  • Untreated hypo- or hyperthyroidism.
  • Uncontrolled liver, kidney or cardiovascular disease or diabetes.
  • Implanted pacemaker or metal implant.
  • History of thrombophlebitis, any hematological disease.
  • No past or present neurological and musculoskeletal disorders that will have affected health condition.
  • No smoking and drinking habits.
  • No psychological problems.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Shymaa Mohammed

    Cairo

Other trials in Egypt

About this study

Official title: Effect of Dry Needling on Insulin Resistance in Obese Post- Menopausal Women

The aim of the study is to determine the effect Dry Needling of on insulin resistance in obese postmenopausal women.

Read the detailed description

Insulin resistance and abdominal obesity have a negative impact on quality of life of postmenopausal women. Obesity and, more specifically, the level of intra-abdominal fat, are positively associated with cardiovascular disease and cardiovascular disease risk factors such as increased plasma lipids and lipoproteins, hyperinsulinemia, and insulin resistance. This study has shown associations among menopause, body fat, and body fat distribution, suggesting that increased abdominal fat distribution could partially mediate the increased cardiovascular disease risk of postmenopausal women .

Abdominal obesity can reflect excess of visceral fat tissue or subcutaneous or both. Visceral fat contributes to the pathogenesis of glucose intolerance and insulin resistance. Insulin resistance is an impaired condition of glucose absorption that induced by insulin .It represents a significant medical and socioeconomic issue impacting women's health and quality of life. So there is clinical experience and documentation for the effectiveness of Dry Needling in the treatment of insulin resistance in obese post-menopausal women.

Being tested
Dry Needle, abdominal exercises, and medical standard care for insulin resistance

What participants receive

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

  • Dry NeedleOther

    Dry Needle has been used to treat obesity. Clinical research has found that it is particularly effective for abdominal fat loss.Dry needling in the abdominal region requires an in-depth understanding of the underlying anatomy due to significant safety risks.

  • abdominal exercises, and medical standard care for insulin resistanceOther

    To reduce belly fat, combine core-strengthening exercises like planks, bicycle crunches, and leg raises with overall fat-burning cardio (walking, running) and a healthy diet

Study groups in NCT07365878
Study groupRoleWhat they receive
Dry NeedleExperimental26 patients who were treated with Dry Needling (three times /week/4 months), abdominal exercises, and medical standard care for insulin resistance.
Receives: Other: Dry Needle; Other: abdominal exercises, and medical standard care for insulin resistance
abdominal exercises and medical standard care for insulin resistance.OtherWhile Group (B), 26 patients treated with abdominal exercises and medical standard care for insulin resistance.
Receives: Other: abdominal exercises, and medical standard care for insulin resistance

What is being measured

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

  1. HOMA-IR

    Outcome measures, HOMA-IR (Homeostasis Model Assessment) will be used to assess insulin resistance. HOMA-IR is a model of interactions between glucose and insulin dynamics that is then used to predict fasting steady-state glucose and insulin concentrations for a wide range of possible combinations of insulin resistance and β-cell function.

    Measured: 4 months

Secondary outcomes (4)
  1. ultrasound

    Abdominal fat thickness will be assessed by ultrasound (Aplio 500-model TUS-A500, fundamentals (2B77-004EN*M)

    Measured: 4 months

  2. BMI by kg/m2

    weight and height will be combined to report BMI in kg/m^2

    Measured: 4 months

  3. waist circumferences by tape

    Measured: 4 months

  4. The surface under the cumulative ranking curve (SUCRA)

    The surface under the cumulative ranking curve (SUCRA) was used to rank and compare the effects of different types of exercise. SUCRA values range from 0 to 100, where 100 indicates the best treatment with no uncertainty and 0 indicates the worst treatment with no uncertainty. Thus, higher SUCRA values indicated the better effects of an exercise intervention prior to and after four-month treatment duration for both groups.

    Measured: 4 months

Timeline

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

  1. First posted26 Jan 2026
  2. Study start1 Jan 2025
  3. Primary completion1 Apr 2025
  4. Study completion1 Dec 2025

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
Crossover
Masking
Single blind
Who is masked
Participant
Enrolment
52 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07365878
Sponsor's protocol ID
P.T.REC/012/006055
Acronym
Dry needle
Status last verified
Jan 2026
First submitted
14 Dec 2025
Last updated
26 Jan 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 Dry Needle in people with Insulin Resistance-abdominal Fats -Post Menopausal Women, 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 8 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 26 Jan 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?

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?

HOMA-IR (time frame: 4 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 26 Jan 2026.

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