Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00974103
Other study ID # 2009/798
Secondary ID 2009/798
Status Completed
Phase N/A
First received September 9, 2009
Last updated August 31, 2012
Start date September 2009
Est. completion date August 2010

Study information

Verified date August 2012
Source Helse Stavanger HF
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Interventional

Clinical Trial Summary

The purpose of this study is to identify how many females have persistent low back pain and/or pelvic pain 3-6 months post partum. The females that have persistent pelvic pain can continue in the study and be examined by a chiropractor. They will then divide the females into Hanne Alberts 5 subgroups of pelvic pain. The females that have one-sided pelvic pain will be invited to participate in a randomised controlled study where chiropractic intervention is compared to exercises.


Description:

The study is a follow up study to "Prevalence of low back pain and pelvic pain in the pregnant population in Stavanger".


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date August 2010
Est. primary completion date August 2010
Accepts healthy volunteers No
Gender Female
Age group 16 Years to 50 Years
Eligibility Inclusion Criteria:

- Low back and\or pelvic girdle pain during pregnancy

- Fluent understanding of spoken and written Norwegian

Exclusion Criteria:

- hospitalisation due to pain or complications post partum

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Intervention

Other:
exercise advise
Exercises
chiropractic treatment and exercises
Manipulation, mobilisation, soft tissue work, ergonomic and exercise advise. Maximum 12 treatments

Locations

Country Name City State
Norway Stavanger university hospital Stavanger

Sponsors (2)

Lead Sponsor Collaborator
Helse Stavanger HF University of Stavanger

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oswestry Disability Index 20 weeks after the initial assessment Yes
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05848479 - Effect of Clamshell Exercise on Lumbopelvic Stability and Low Back Pain in Post Partum Women N/A