Viewing Study NCT06640543



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06640543
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-10-11

Brief Title: Effect of Kinesiotape Versus Myofascial Release on Postnatal Low Back Pain
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of Kinesiotape Versus Myofascial Release on Postnatal Low Back Pain a Randomised Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study aims to determine the difference between the effect of kinesiotape and myofascial release in the treatment of postnatal low back pain
Detailed Description: Postpartum back pain may occur in up to 44 of women after childbirth People who have chronic back pain may have a limited range of motion andor tenderness upon touch

Therapeutic KT can benefit a wide variety of musculoskeletal and sports injuries plus inflammatory conditions According to the Kinesiotape Method Manual this traction promotes an elevation of the epidermis and reduces pressure on the mechanoreceptors located below the dermis thereby reducing nociceptive stimuli and low back pain

Myofascial release MFR is a treatment that uses gentle pressure and stretching to facilitate the release of fascial restrictions caused by accidents injury stress repetitive use and traumatic or surgical scarring

Myofascial release is a form of soft tissue therapy used to treat somatic dysfunction and accompanying pain and restriction of motion This is accomplished by relaxing the contracted muscle increasing circulation increasing venous and lymphatic drainage and stimulating the stretch reflex of muscles and overlying fascia so reducing low back pain

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None