Ignite Creation Date:
2024-05-06 @ 7:56 PM
Last Modification Date:
2024-10-26 @ 3:17 PM
Study NCT ID:
NCT06198348
Status:
COMPLETED
Last Update Posted:
2024-04-19
First Post:
2023-12-26
Brief Title:
Aerobic Training With and Without Resistance Training in Polycystic Ovarian Syndrome
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Effects of Aerobic Training With and Without Resistance Training on Waist to Hip Ratio Quality of Life and Menstrual Dysfunction in Polycystic Ovarian Syndrome
Status:
COMPLETED
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Polycystic ovary syndrome PCOS characterized by a chronic disorder in ovulation along with hyperandrogenism has become one of the most common endocrine disorders in women of reproductive age with an estimated 5-15 prevalence It has the symptoms such as menstrual disorders infertility hyperandrogenism obesity hirsutism and acne PCOS is linked to Psychological morbidities eg increased risk of stress depression low self-esteem poor body image and reduced health-related quality of life Approximately 75 of people with PCOS have a fat accumulation in the central area of the body
Detailed Description:
A Randomized controlled trial will be conducted to determine the effects of Aerobic training with and without resistance training on the waist to hip ratio QoL and menstrual dysfunction in polycystic ovarian syndrome A sample size of 22 PCOS womens will be taken Data will be collected from Jinnah Hospital Lahore by using PCOSQ and SF-36 questionnaire A written consent form will be taken from participants meeting inclusion criteria and will be randomly allocated into two groups of equal members One group undergoing aerobic with resistance exercise training ie the experimental group and other with aerobic exercise ie control group The interventions will be provided for 30 mints for 3 days per week for 2 months All participants in both groups will be evaluated before and after the treatment programs
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None