- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07566715
Pilates vs Aerobic Exercises on Vitamin D and Ionized Calcium in Postnatal
April 30, 2026 updated by: Adly A Adam
Effect of Pilates Versus Aerobic Exercises on Vitamin D Level and Ionized Calcium in Postnatal Women
Vitamin D and calcium levels are negatively affected during postpartum period, making postnatal woman more vulnerable to health issues and consequently lowering her quality of life.
Twelve-weeks of Pilates training have improved serum 25-hydroxy vitamin D levels and changed anthropometry in inactive overweight women.
It is well-known globally that aerobic exercise is low to moderate-intensity physical activity.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
This study will be conducted to determine the difference between the effect of Pilates and aerobic exercises on serum levels of vitamin D, ionized calcium and osteocalcin in postnatal women.
The practical aspect of the study will be conducted at the Out Patient Clinic of Al-Zahraa University Hospital, Al Azahar University, Cairo, Egypt.
Sixty postnatal women will participate in this study.
Their ages range will be from 18 to 40 and their BMI range will be from 25-35 kg/ m².
All women will be postnatal period by 6-12 weeks, as well healthy primipara or multipara.
The participants will be randomly assign into two equal groups by using a sealed envelope method; group A (Pilates exercises group) will include thirty postnatal women, whom will perform Pilates exercises for 12 weeks, and group (B), (Aerobic exercises group)will include thirty postnatal women, whom will perform aerobic exercises program for 12 weeks.
Will assess vitamin D, Ionized calcium and osteocalcin for all participants at the start and after the treatment program, then will statistically analyze the data.
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ahmed A Tolba, M.Sc.
- Phone Number: 105 +20100352075
- Email: eth.com@pt.cu.edu.eg
Study Contact Backup
- Name: Afaf M Botla, Professor
- Phone Number: 105 +20100352075
- Email: eth.com@pt.cu.edu.eg
Study Locations
-
-
Al Zahraa University Hospital
-
Cairo, Al Zahraa University Hospital, Egypt, 11731
- AlZahraa University Hospital
-
Contact:
- Mohamed A Awad, Professor
- Phone Number: 105 +20100135075
- Email: eth.com@pt.cu.edu.eg
-
Contact:
- Afaf M Botla, Professor
- Phone Number: 105 +20100135075
- Email: eth.com@pt.cu.edu.eg
-
Principal Investigator:
- Ahmed A Tolba, M.S.c
-
Sub-Investigator:
- AbdelHamid A AttaAllah, PRofessor
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Their ages were ranged from 18-40 years old.
- Their body mass index (BMI) was ranged from 25-35 kg/ m².
- They were postnatal period by 6-12 weeks.
- They were primipara or multipara.
- They were healthy postpartum women.
Exclusion Criteria:
- High risk pregnant history.
- Sever postpartum complications.
- Cardiovascular diseases i.e., utilizing pace maker.
- Skeletal deformity.
- Participation at any other exercise training program during this study.
- Malignant conditions.
- History of acute infection
- Neurological problem; epileptic fits…etc.
- Mental problem to prevent evaluation and cooperation.
- Renal, liver or endocrinal disorders.
- Pulmonary disorders.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group A (Pilates exercises group)
Experimental Group A (Pilates exercises group) will be thirty postnatal women will perform Pilates exercises for 12 weeks, 3 sessions per week for 60 minutes
|
Pilates exercises program will include twelve movements: Bridging, Roll Up, Pilates Hundred, One Leg Circle (both ways), Single Straight Leg Stretch, Double Leg Stretch, Spine Stretch Forward Single Leg Kick, Side Kick up and down, Side Kick circles, Curling.
20 minutes walking on the treadmill at moderate intensity (70% of the maximal heart rate).
|
|
Experimental: Experimental Group B(Aerobic exercises group)
Experimental Group B(Aerobic exercises group) will be thirty postnatal women will perform aerobic exercises for 12 weeks, 3 sessions per week for 60 minutes
|
Pilates exercises program will include twelve movements: Bridging, Roll Up, Pilates Hundred, One Leg Circle (both ways), Single Straight Leg Stretch, Double Leg Stretch, Spine Stretch Forward Single Leg Kick, Side Kick up and down, Side Kick circles, Curling.
20 minutes walking on the treadmill at moderate intensity (70% of the maximal heart rate).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vitamin D serum level
Time Frame: At baseline, and Immediately post-intervention
|
High-performance liquid chromatography (Shimadzu, Japan) was used to assess 25(OH)D serum levels before and after the study program in both groups, using 25-OH vitamin D ELISA.
Kits (Life Sciences Inc. USA).
Values of 25(OH)D < 20 ng/ml are considered deficient, values ranged 21 to 29 ng/ml are considered insufficient, and 30 ng/ml is considered ideal
|
At baseline, and Immediately post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ionized calcium serum level
Time Frame: At baseline, and Immediately post-intervention
|
serum ionized calcium levels measured before and after the intervention, using Easy Lyte Ca analyzer (USA) which utilizes ISE (Ion Selective Electrode) technology in order to measure electrolyte.
The manufacturer's instructions were followed at all times.
In adults (18-60 years), the reference value of serum calcium is 1.05-1.3
mmol/L
|
At baseline, and Immediately post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Mohamed A Awad, Professor, Cairo University
- Study Chair: AbdelHamid A AttalAllah, Professor, AlZahraaUniversity
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 30, 2026
Study Registration Dates
First Submitted
April 25, 2026
First Submitted That Met QC Criteria
April 30, 2026
First Posted (Actual)
May 5, 2026
Study Record Updates
Last Update Posted (Actual)
May 5, 2026
Last Update Submitted That Met QC Criteria
April 30, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/006316
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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