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Effects of Breathing Exercises in Women With Chronic Pelvic Pain

Investigation of the Clinical Effects of Breathing Exercises Combined With Pelvic Floor Exercises in Women With Chronic Pelvic Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05875545
Enrollment
20
Registered
2023-05-25
Start date
2023-06-01
Completion date
2024-06-01
Last updated
2024-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pelvic Pain Syndrome, Pelvic Floor; Relaxation, Breathing Exercises, Women

Keywords

Women with Chronic Pelvic Pain, Breathing Exercises, Pelvic Floor Exercises

Brief summary

The primary cause of the complex interaction of chronic pelvic pain originates from the visceral organs in the pelvic cavity, and it has been observed that musculoskeletal dysfunctions (such as increased muscle activity in the pelvic floor muscles) are often accompanied by visceral painful stimuli in the pelvic region as a result of shared innervation and visceral-somatic convergence. This study aims to investigate the effect of breathing exercises combined with pelvic floor exercises on pain, pelvic floor muscle activity, psychological factors, and quality of life in women with chronic pelvic pain.

Interventions

OTHERBreathing Exercises

Diaphragmatic breathing exercises with a physiotherapist for 8 weeks, two days a week

Pelvic floor exercises with a physiotherapist for 8 weeks, two days a week

Sponsors

Saglik Bilimleri Universitesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Be diagnosed with chronic pelvic pain (CPA) * Having pelvic pain for at least 6 months * 18-45 years old * Having high resting activity of the pelvic floor (\>2 microvolts based on superficial EMG (sEMG) readings)

Exclusion criteria

* Having a history of pelvic cancer and/or surgery * Receiving radiotherapy and/or chemotherapy * Having a neurological and/or psychiatric pathology * Have a urinary tract infection * Menopause * Presence of current pregnancy status * History of miscarriage and ectopic pregnancy * Presence of prolapse * Being \>30 kg/cm2 according to body mass index (BMI) * Have received treatment for the pelvic area including manual therapy and electrotherapy in the last 6 months * Having had botulinum toxin injections in the pelvic region in the last 6 months * Having a communication problem

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Pelvic Floor Muscle Activity (PFMA) at 8 weeksat the baseline and end of the 8 weeks (16 sessions)PFMA measurement will be performed with the sEMG NeuroTrac MyoPlus Pro (Verity Medical Ltd, UK) device integrated with computer software for digital analysis and report generation.
Change from Baseline Visual Analogue Scale (VAS) at 8 weeksat the baseline and end of the 8 weeks (16 sessions)Pain severity will be evaluated with the VAS.
Change from Baseline McGill Pain Scale- Short Form at 8 weeksat the baseline and end of the 8 weeks (16 sessions)The scale consists of 3 parts. In the first part of the scale, a total of 3 pain scores are obtained: sensory pain score, perceptual pain score and total pain score. In the second part, there were five word groups ranging from mild pain to unbearable pain to determine the severity of the patient's pain. In the third part, the current pain intensity of the patient was evaluated using a visual comparison scale.

Secondary

MeasureTime frameDescription
Short Form-36at the baseline and end of the 8 weeksEvaluation of quality of life
Global Pelvic Floor Disorder Questionnaireat the baseline and end of the 8 weeksGlobal pelvic floor disorders will be evaluated at baseline and after 8 weeks
Depression, Anxiety and Stress Scaleat the baseline and end of the 8 weeksEvaluation of moods (depression, anxiety and stress)
Corbin Postural Rating Scaleat the baseline and end of the 8 weeksMeasuring of posture changes
Pelvic Pain Impact Questionnaireat the baseline and end of the 8 weeksClinical evaluation of pelvic pain effect

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026