Effect Of Treadmill Based Aerobic Exercise Intervention On Menstruation And Quality Of Life In Women With Polycystic Ovarian Syndrome

NCT ID: NCT04744948

Last Updated: 2021-02-23

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-01

Study Completion Date

2022-02-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

this study will be carried to investigate the effect of aerobic exercise on menstrual regularity and quality of life in pco women

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This study will be carried out on sixty females with polycystic ovarian syndrome (PCOS) patients will be randomly assigned into two equal groups: control group (30 women) will receive low caloric diet 1200 Cal/day) while study group (30 women) will receive the same diet regime and treadmill aeobic exercise

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Polycystic Ovary Syndrome Irregular Menses

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

control group receive low caloric diet study group receive high intensity interval training
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

low caloric diet

low caloric diet 1200cal/day

Group Type PLACEBO_COMPARATOR

low caloric diet

Intervention Type OTHER

low caloric diet (1200ca/lday)

treadmill

treadmill aerobic exercise training

Group Type EXPERIMENTAL

Treadmill exercise

Intervention Type DEVICE

high intensity interval training

low caloric diet

Intervention Type OTHER

low caloric diet (1200ca/lday)

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Treadmill exercise

high intensity interval training

Intervention Type DEVICE

low caloric diet

low caloric diet (1200ca/lday)

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* women with pco
* age from17 to 28 years
* BMI 25- 30

Exclusion Criteria

* Asthma and chronic respiratory disease
* congenital spinal problems
* cardiopulmonary disease
* physical impairments
Minimum Eligible Age

17 Years

Maximum Eligible Age

28 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Miral Saleh Mohamed

assistant lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

fahema m okiel, phd

Role: STUDY_DIRECTOR

Cairo University

amal mo youssef, phd

Role: STUDY_CHAIR

Cairo University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Cairo University

Cairo, , Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

miral m saleh, md

Role: CONTACT

01200678845 ext. +012

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

miral s mohamed, md

Role: primary

01200678845 ext. +012

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ETMQWP

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.