Insulin Sensitivity Response to High-Intensity Training in Insulin Resistance During Pregnancy

NCT ID: NCT04830995

Last Updated: 2023-01-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-03-24

Study Completion Date

2020-11-01

Brief Summary

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Insulin Resistance is one of the common complications that occur during pregnancy. Early intervention is essential to prevent the development of the diseaseThere is evidence that physical inactivity increases the risk of a lot of adverse health problems, including coronary heart disease, type 2 diabetes, breast and colon cancers. It also shortens life expectancy. Pregnancy is a period in the life of women that is often associated with decreased daily physical activity and decreased participation in sports and exercise . In the first few weeks of pregnancy, maternal carbohydrate metabolism is affected by a rise in maternal levels of estrogen and progesterone that stimulates pancreatic β-cell hyperplasia and insulin secretion. As pregnancy progress, pancreatic islet cell hypertrophy continues and there is an increased insulin response to glucose or meal stimulation.

Detailed Description

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This study was carried out upon twenty multigravida pregnant female between 5-6 months gestation with IR calculated by HOMA test (fasting blood glucose× fasting insulin) ÷ 22.5. Fasting blood glucose was assessed by the method approved by (7, 13) .The test materials for this method were supplied as kits by "Diamond Diagnostics," while Insulin concentrations were stated in formerly frozen and defrosted serum samples by enzyme immunoassay using the human Insulin ELISA kits.

Conditions

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High Intensity Interval Training Diet, Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

group (A) received HIIT and low diet for four weeks, 3 sessions weekly. While the control group received diet only.
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators
Randomization was done by sealed envelope

Study Groups

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diet program

moderate restricted diet (1800-2000 kcal/day) for four weeks, 3 sessions weekly

Group Type EXPERIMENTAL

moderate restricted diet (1800-2000 kcal/day) for four weeks

Intervention Type DIETARY_SUPPLEMENT

high intensity interval training 3 sessions for four weeks

high intensity interval training

high intensity interval training for four weeks, 3 sessions weekly

Group Type EXPERIMENTAL

moderate restricted diet (1800-2000 kcal/day) for four weeks

Intervention Type DIETARY_SUPPLEMENT

high intensity interval training 3 sessions for four weeks

Interventions

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moderate restricted diet (1800-2000 kcal/day) for four weeks

high intensity interval training 3 sessions for four weeks

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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high intensity interval training

Eligibility Criteria

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Inclusion Criteria

* forty multigravida females.
* their age ranged between 25 to 35 years old.
* Body mass index (BMI) \<30kg/ m².

Exclusion Criteria

* females with pelvic pathology as endometriosis.
* females have irregular menstrual cycles.
Minimum Eligible Age

25 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Heba mohamed Embaby

UNKNOWN

Sponsor Role collaborator

Salwa Elgendy

UNKNOWN

Sponsor Role collaborator

Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Ghada Ebrahim El Refaye

assistant professor Department of Physical Therapy for Women's Health, Faculty of Physical therapy, Cairo University, Egypt

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ghada Elrefaye

Giza, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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Cairo Un100

Identifier Type: -

Identifier Source: org_study_id

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