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Active, not recruitingNCT07871175Updated Oct 13, 2026

Inspiratory Muscle Training for the Management of Polyendocrine Metabolic Ovarian Syndrome

An interventional study of Exercise in Poly Cystic Ovary Syndrome, sponsored by British University In Egypt. Active, not recruiting at 1 site in Egypt. Open to female participants aged 20 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by British University In Egypt · Not applicable, Interventional, and Treatment

Updated Oct 13, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
20 Years to 30 Years
Sex
Female
01

Study summary

Inspiratory muscle training (IMT) is a relatively simple and accessible form of exercise that specifically targets the respiratory muscles and has been reported to improve inspiratory muscle strength, respiratory efficiency, exercise capacity, and autonomic cardiovascular regulation in different populations. Given the close relationship between respiratory muscle function, exercise capacity, autonomic regulation, and metabolic health, IMT may represent a potentially useful adjunctive intervention for women with PCOS. Therefore, investigating the effects of inspiratory muscle training on relevant metabolic, functional, and clinical outcomes in women with PCOS may provide an additional therapeutic approach within physiotherapy and lifestyle-based management.

02

Conditions studied

  • Poly Cystic Ovary Syndrome

Keywords

  • polycystic ovary syndrome
03

In context

Polycystic Ovary Syndrome

975 studies on the registry are indexed under Polycystic Ovary Syndrome; 177 are open to participants now.

This study's planned enrollment of 40 is below the median of 70 across 710 interventional studies indexed under Polycystic Ovary Syndrome.

Browse Polycystic Ovary Syndrome studies →

Lead sponsor

British University In Egypt is the lead sponsor of 69 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 30 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Polycystic ovarian syndrome

Exclusion criteria

Exclusion Criteria:

  • pelvic tumors
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    inspiratory muscle training

    Participants performed inspiratory muscle training using a The POWER breathe equipment (POWER breathe International Ltd.) at 50% of maximal inspiratory pressure (MIP). Training consisted of two sets of 30 inspiratory efforts per day, performed 5 days per week for 8 weeks. MIP was reassessed weekly, and the training resistance was adjusted to maintain an intensity corresponding to 50% of the current MIP. Participants performed the training in a standardized seated position following standardized breathing instructions.

    Other: Exercise

  • Sham comparator
    Sham IMT control group

    Participants allocated to the sham group used the same threshold inspiratory loading device with the inspiratory resistance set at 10% of MIP. They performed the same training schedule as the intervention group (two sets of 30 inspiratory efforts per day, 5 days per week for 8 weeks) and received identical instructions and follow-up procedures. The sham resistance was maintained at a minimal level insufficient to induce a meaningful inspiratory muscle-training stimulus.

    Other: Exercise

Interventions

  • OtherExercise

    Training consisted of two sets of 30 inspiratory efforts per day, performed 5 days per week for 8 weeks. MIP was reassessed weekly, and the training resistance was adjusted to maintain an intensity corresponding to 50% of the current MIP. Participants performed the training in a standardized seated position following standardized breathing instructions.

06

What researchers measure

Primary outcomes

  1. Homeostatic model assessment of IR (HOMA- IR),

    Time frame: 8 weeks

Secondary outcomes

  1. Hormonal profile (FSH, LH, FSH-LH ratio)

    Time frame: 8 weeks

  2. Serum triglyceride (TG)

    Time frame: 8 weeks

  3. HDL

    Time frame: 8 weeks

  4. LDL

    Time frame: 8 weeks

07

Study locations

1 site
  • British university in cairo
    Cairo, Cairo Governorate 11835, Egypt
08

References and documents

Publications

  • Reed BL, Tavoian D, Bailey EF, Funk JL, Coletta DK. Inspiratory muscle strength training to improve cardiometabolic health in patients with type 2 diabetes mellitus: protocol for the diabetes inspiratory training clinical trial. Front Endocrinol (Lausanne). 2024 Sep 13;15:1383131. doi: 10.3389/fendo.2024.1383131. eCollection 2024. PubMed 39345888 ↗

Related links

Individual participant data

Plan to share: Undecided

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2026 (actual). Primary completion is estimated for Dec 2026, 1 month after the start.

Of 206 non-industry interventional studies with no phase under Polycystic Ovary Syndrome, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 35. This study's planned 1 month is below that.

Counting every sponsor, half of 221 studies reached it within 18 months; a quarter within 7 and three quarters within 35.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 7, 2026
First posted
Oct 13, 2026
StartActual
Oct 7, 2026
Primary completionEst.
Dec 2, 2026
CompletionEst.
Dec 10, 2026
Last update
Oct 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07871175
Lead sponsor
British University In Egypt
Responsible party
Miral saleh (Lecturer, British University In Egypt) — Principal investigator
First posted
Oct 13, 2026
Start date
Oct 7, 2026
Primary completion
Dec 2, 2026 (estimated)
Completion
Dec 10, 2026 (estimated)
Last update
Oct 13, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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