Kinesio Taping With &Without Craniosacral Therapy in Pregnant Females With SIJ Dysfunction.

Sacral Disorder Clinical Trial

Official title:

Effect of Kinesio Taping With and Without Craniosacral Therapy on Pain, Disability, and Quality of Life in Pregnent Female With Sacroiliac Joint Dysfunction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05811325
• Other study ID #: REC/RCR&AHS/22/0538
• Status: Completed
• Phase: N/A
• Start date: February 11, 2022
• Est. completion date: January 30, 2023

Study information

• Verified date: March 2023
• Source: Riphah International University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

SIJ dysfunction adversely affects quality of life and causes functional impairment and disability. Although, K taping and craniosacral therapy were previously affective in treating SI joint dysfunction, the combined affects of these intervention have not been compared previously to K taping alone.

Description:

This study is a randomized controlled trial and have 30 pregnant women suffering from SIJH dysfunction. There is 2 groups and both have received treatment for 6 weeks. The data on pain is collected through VAS and the data on disability is collected through Oswestry Disability Index, and data on quality of life will be collected using SF-36. Measurements will be taken at the beginning of the study and at the end of the 4th week, at the completion of the study. Data will be analyzed using SPSS.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: January 30, 2023
• Est. primary completion date: December 30, 2022
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

• age between 18-35
• pregnant females in 3rd trimester
• pregnant females with SIJ dysfunction

Exclusion Criteria:

• high risk pregnancy
• pregnant females with hypermobility syndrome
• previous pelvic history

Related Conditions & MeSH terms

• Sacral Disorder

Intervention

Other:
• kinesiotaping without craniosacral therapy
The first treatment group will receive kinesio taping for 6 weeks atleast 4 times per week
• kinesiotaping with craniosacral therapy
The second treatment group will receive kinesio taping with craniosacral therapy for 6 weeks atleast 4 times per week with each session lasting for 60 minutes

Locations

Country	Name	City	State
Pakistan	Mayo Hopital	Lahore

Sponsors (1)

Lead Sponsor	Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	VISUAL ANALOGUE SCALE	This scale is used to assess pain.	6 WEEKS
Primary	Oswestry Disability Index	it is used to measure disability.	4 weeks
Secondary	SF-36	Data on quality of life is measured by this scale.	4 weeks