Viewing Study NCT06377618



Ignite Creation Date: 2024-05-06 @ 8:25 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06377618
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-04-22
First Post: 2024-04-17

Brief Title: Comparison Of Resistance Training And Core Strengthening Exercises Vitamin D In Postmenopausal Women With Low Back Pain
Sponsor: Superior University
Organization: Superior University

Study Overview

Official Title: Comparison Of Resistance Training And Core Strengthening Exercises Along With Vitamin D Intake In Postmenopausal Women With Low Back Pain
Status: ACTIVE_NOT_RECRUITING
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: This study aims to evaluate the effectiveness of resistance training core strengthening exercises and vitamin D supplementation in reducing low back pain LBP among postmenopausal women
Detailed Description: Postmenopausal women are particularly susceptible to LBP due to physiological changes such as reduced estrogen levels decreased muscle mass and bone density The randomized controlled trial RCT will be conducted over six months in various clinical settings in Lahore with a sample size of 36 participants divided into two groups The inclusion criteria focus on postmenopausal women aged 50-70 years experiencing LBP for at least three months and who are not currently taking vitamin D supplements Data on pain intensity functional disability muscle strength endurance and vitamin D levels will be collected and analyzed to assess the interventions impact The studys findings could provide evidence-based recommendations for managing LBP in postmenopausal women combining physical activity with nutritional supplementation

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