Comparative Effects of Neurodynamic Stretch and Myofascial Pain Release in Polycystic Ovarian Syndrome.

Riphah International University

Status: Enrolling

Conditions: Polycystic Ovarian Syndrome

Treatments: Other: Neurodynamic stretches; Other: myofascial pain release technique Interventions:

Study type: Interventional

Funder types: Other

Identifiers

NCT07645014

REC/PCR & AHS/25/0515

Details and patient eligibility

About

The study will be a non-blinded randomized controlled trial, consisting of two groups. Non-probability Convenience sampling will be used to recruit participants who will meet the inclusion criteria. Group allocation will be performed using the sealed envelope method to ensure randomization of participants into experimental and control groups. The sample size will be 38 (19 in each group). Group A will receive neurodynamic stretches while Group B will receive myofascial pain release technique.

Full description

The most prevalent endocrinopathy in women of reproductive age is polycystic ovarian disorder (PCOS), with notable clinical characteristics related to reproduction, metabolism, dermatology, and psychology. Among the most prominent gynecological disorders in women is dysmenorrhea, which has a major detrimental effect on one's quality of life. This randomized clinical study aims to evaluate and compare the effects of neurodynamic stretching combined with diaphragmatic breathing versus myofascial pain release therapy in reducing the intensity and duration of dysmenorrhea in girls with PCOS, to assess the impact of both interventions on improving the quality of sleep among girls with PCOS and to compare the effects of neurodynamic stretching with diaphragmatic breathing and myofascial pain release therapy on enhancing functional mobility in females with PCOS.

The study will be a non-blinded randomized controlled trial, consisting of two groups. Non-probability Convenience sampling will be used to recruit participants who will meet the inclusion criteria. Group allocation will be performed using the sealed envelope method to ensure randomization of participants into experimental and control groups. The sample size will be 38 (19 in each group). Group A will receive neurodynamic stretches which includes abdominal stretches, calf stretches, hamstring stretches. Group B will receive myofascial pain release technique. The study will be conducted over a period of 10 months at Shaikh Zayed Hospital Lahore. Ethical approval will be obtained. Individuals fulfilling the inclusion criteria will be selected, followed by written informed consent after explaining the study purpose. Participants will then be randomly allocated to one of the two groups. Comparative Training would be performed thrice a week on alternate days for a total duration of 6 weeks. Total sessions will be 18. All outcome measurements will be performed pre and after the 6 weeks' intervention period.

Enrollment: 38 estimated patients

Sex: Female

Ages: 18 to 35 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• • Age 18-35 years

  • Diagnosed cases of PCOS
  • Irregular periods until 3 months.
  • Presence of dysmenorrhea (Check WaLIDD Questionnaire)
  • BMI
  • Age of Menarche (13 years)

Exclusion criteria

• • History of endocrine disorders

  • Endometriosis
  • Tumour
  • Any major surgeries
  • Marital Status (un married)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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38 participants in 2 patient groups

Neurodynamic stretches

Active Comparator group

Description:

Group A will receive neurodynamic stretches which includes abdominal stretches, calf stretches, hamstring stretches.

Treatment:

Other: Neurodynamic stretches

myofascial pain release technique

Experimental group

Description:

Group B will receive myofascial pain release technique.

Treatment:

Other: myofascial pain release technique Interventions: