Comparative Effects of Hypopressive Exercises and Paula Method in Postpartum Women.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age25-40
SponsorRiphah International University

About this trial

This study will be a randomized clinical trial with a sample size of 60 postpartum females. The setting of the study will be Bilal Medicare, Sargodha. 60 postpartum women will be included based on age, parity, mode of delivery and type of urinary incontinence. Women with primary gravida, cesarean section and urge and mixed urinary incontinence will be excluded. This study aims to compare the effectiveness of Hypopressive Exercises and the Paula Method in improving urinary incontinence severity, pelvic floor muscle strength and quality of life in postpartum women. Patients of both groups receive two treatment sessions per week over an 8-week period. Group A will be given Hypopressive exercise and Group B will be given Paula exercise protocol. Both groups will perform a standardized kegel exercises for pelvic floor muscle activation and strengthening as baseline treatment followed by their assigned interventions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

• Multipara women from 25-40 years

Six weeks postpartum

Vaginal delivery method

Reported ≥1 episodes of urine leakage per week

Disqualifiers

• No pelvic floor physiotherapy in last 6 months

Patients with any medical and gynaecological risk factors and /or conditions

Patients with any neurological problems, urinary tract infection, diabetes mellitus, hepatitis and ascites

Pelvic surgery in last 6 months

Trial design

Design model

Parallel

Treatments tested in this trial

  • Hypopressive exercise

    Other intervention

    (n=30) Each participant will receive treatment with hypopressive exercises for entire 08 weeks' intervention period.

  • Paula exercise

    Other intervention

    Each participant will receive treatment with the Paula method for entire 08 weeks' intervention period.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Hypopressive exerciseActive comparator 1 intervention
Group B: Paula exerciseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

International Consultation on Incontinence Questionnaire - Urinary Incontinence Short Form (ICIQ-UI SF)

The ICIQ-UI SF is a standardized and internationally recognized tool for assessing the severity of urinary incontinence and its impact on quality of life. It consists of 4 questions; frequency of leakage, amount of urine lost, overall impact on daily life and self-diagnostic items (non-scored).

Time frame
8 weeks
2

Modified Oxford Grading Scale (Manual Muscle Testing of Pelvic Floor)

This clinical scale is used to assess pelvic floor muscle strength through vaginal palpation, grading the strength from 0 (no contraction) to 5 (strong contraction). It helps determine the baseline function and progress of pelvic floor rehabilitation. The scale uses a single-item score ranging from 0 to 5, based on the therapist's tactile evaluation of the pelvic floor contraction. Though subjective, its validity is supported through clinical correlation with manometric and EMG readings. It is especially useful in low-resource settings where instrumentation is unavailable.

Time frame
8 weeks
3

Urinary Incontinence Impact Questionnaire - 7 (UIQ-7)

The UIQ-7 is a subscale of the PFIQ-7 and is used to evaluate the impact of urinary incontinence on daily activities and social functioning. It is especially useful for measuring the subjective burden of incontinence on the patient's life. The UIQ-7 consists of 7 questions, each scored on a scale of 0 (not at all) to 3 (quite a bit), with a total score ranging from 0 to 21. Higher scores indicate greater impact on quality of life.

Time frame
8 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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