Skip to main content
OpenTrials
Completed

NCT Number: NCT05811325

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Sacral Disorder

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Hopital

Lahore, Pakistan

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

kinesiotaping without craniosacral therapy

Other

The first treatment group will receive kinesio taping for 6 weeks atleast 4 times per week

kinesiotaping with craniosacral therapy

Other

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

Primary outcomes

  1. VISUAL ANALOGUE SCALE

    Time frame: 6 WEEKS

    This scale is used to assess pain.

  2. Oswestry Disability Index

    Time frame: 4 weeks

    it is used to measure disability.

Secondary outcomes

  1. SF-36

    Time frame: 4 weeks

    Data on quality of life is measured by this scale.

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2022
Study completion
2023
First posted
Apr 13, 2023
Registry last updated
Apr 13, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.