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Postnatal WomenNCT07566715

Pilates vs Aerobic Exercises on Vitamin D and Ionized Calcium in Postnatal

A study testing Exercise in people with Postnatal Women and Vitamin D, run by Adly A Adam at 2 sites in Egypt.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 40 years, women onlyHealthy volunteers can take part
Conditions the study is for
Postnatal Women, Vitamin D
What is being tested?
Exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
2 sitesEgypt
Study dates
1 May 2026to 30 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 18 to 40 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • 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.
Show all 11Show fewer
  • History of acute infection
  • Neurological problem; epileptic fits…etc.
  • Mental problem to prevent evaluation and cooperation.
  • Renal, liver or endocrinal disorders.
  • Pulmonary disorders.

Trial locations and contacts

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

Ahmed A Tolba, M.Sc. contact

+20100352075 ext. 105

eth.com@pt.cu.edu.eg

Afaf M Botla, Professor contact

+20100352075 ext. 105

eth.com@pt.cu.edu.eg

Egypt2 sites
  • AlZahraa University Hospital

    Cairo, Al Zahraa University Hospital, 11731

    Afaf M Botla, Professor, 00201001352075 ext. 105, eth.com@pt.cu.edu.eg

    Mohamed A Awad, Professor, 00201001352075 ext. 105, eth.com@pt.cu.edu.eg

  • AlZahraa University Hospital

    Cairo, Al Zahraa University Hospital, 11731

    Mohamed A Awad, Professor, +20100135075 ext. 105, eth.com@pt.cu.edu.eg

    Afaf M Botla, Professor, +20100135075 ext. 105, eth.com@pt.cu.edu.eg

Other trials in Egypt

About this study

Official title: 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.

Read the 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.

Being tested
Exercise

What participants receive

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

  • ExerciseOther

    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.

  • ExerciseOther

    20 minutes walking on the treadmill at moderate intensity (70% of the maximal heart rate).

Study groups in NCT07566715
Study groupRoleWhat they receive
Experimental Group A (Pilates exercises group)ExperimentalExperimental Group A (Pilates exercises group) will be thirty postnatal women will perform Pilates exercises for 12 weeks, 3 sessions per week for 60 minutes
Receives: Other: Exercise
Experimental Group B(Aerobic exercises group)ExperimentalExperimental Group B(Aerobic exercises group) will be thirty postnatal women will perform aerobic exercises for 12 weeks, 3 sessions per week for 60 minutes
Receives: Other: Exercise

What is being measured

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

  1. Vitamin D serum level

    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

    Measured: At baseline, and Immediately post-intervention

Secondary outcomes (1)
  1. Ionized calcium serum level

    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

    Measured: At baseline, and Immediately post-intervention

Timeline

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

  1. First posted5 May 2026
  2. Study start1 May 2026 (estimated)
  3. Primary completion1 Dec 2026 (estimated)
  4. Study completion30 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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
Prospective, clinical randomized study
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07566715
Sponsor's protocol ID
P.T.REC/012/006316
Status last verified
Apr 2026
First submitted
25 Apr 2026
Last updated
5 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Exercise in people with Postnatal Women and Vitamin D, run by Adly A Adam at 2 sites 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 5 inclusion and 11 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: opening soon, as of the sponsor's last update on 5 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 2 sites 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 Ahmed A Tolba, M.Sc. (+20100352075 ext. 105, eth.com@pt.cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Vitamin D serum level (time frame: At baseline, and Immediately post-intervention). 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 5 May 2026; AzTrials last refreshed its copy on 26 Oct 2026.

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