The Effects of Sacroiliac Joint Dysfunction on Gait and Disability

Sponsor
Kutahya Health Sciences University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05786118
Collaborator
(none)
60
1
3.3
18.1

Study Details

Study Description

Brief Summary

It has been reported that gait coordination changes in patients with chronic low back pain, walking slower, taking shorter steps and having asymmetrical stride lengths compared to their healthy peers. In addition to many factor cause gait dysfunction, sacroiliac joint dysfunction might be one of reason of these problems. A study examining the effects of sacroiliac joint dysfunction on gait and disability in individuals with chronic low back pain has not been found in the literature. Therefore, the aim of this study is to evaluate the gait parameters and disability of individuals with chronic low back pain and to reveal their relationship with sacroiliac joint dysfunction.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
The Effects of Sacroiliac Joint Dysfunction on Gait and Disability in Patients With Chronic
Anticipated Study Start Date :
Mar 21, 2023
Anticipated Primary Completion Date :
May 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
SIJ Group

Individuals with sacroiliac joint dysfunction: Participants will be grouped as positive sacroiliac joint dysfunction according to Laslett's algorithm using provocation tests to detect sacroiliac joint dysfunction.

Other: No intervention
There is no intervention in this study

Control Group

Individuals with no sacroiliac joint dysfunction: Individuals with sacroiliac joint dysfunction: Participants will be grouped as negative sacroiliac joint dysfunction according to Laslett's algorithm using provocation tests to detect sacroiliac joint dysfunction.

Other: No intervention
There is no intervention in this study

Outcome Measures

Primary Outcome Measures

  1. Gate speed of time-distance gait parameters [1 minutes]

    Gate speed will be evaluated using with gait platform. The software gives the outcome as km/h.

  2. Step length of time-distance gait parameters [1 minutes]

    Step lengt will be evaluated using with gait platform. The software gives the outcome as cm and calcules for each lower extremity.

  3. Stride length of time-distance gait parameters [1 minutes]

    Stride length will be evaluated using with gait platform.The software gives the outcome as cm.

  4. Step time of time-distance gait parameters [1 minutes]

    Step time will be evaluated using with gait platform.The software gives the outcome as sec and calcules for each lower extremity.

  5. Stride time of time-distance gait parameters [1 minutes]

    Stride time will be evaluated using with gait platform.The software gives the outcome as sec and calcules for each lower extremity.

  6. Cadance of time-distance gait parameters [1 minutes]

    Cadance time will be evaluated using with gait platform.The software gives the outcome as steps/min.

  7. Center of Pressure path length of balance parameters [2 minutes]

    Center of Pressure path length will be evaluated using with gait platform. The software gives the outcome as mm.

  8. Ellipse area of balance parameters [1 minutes]

    Ellipse area will be evaluated using with gait platform. The software gives the outcome as mm2.

Secondary Outcome Measures

  1. Oswestry Disability Index [5 minutes]

    The Oswestry Disability Index (ODI) is an index derived from the Oswestry Low Back Pain Questionnaire used by clinicians and researchers to quantify disability for low back pain. The self-completed questionnaire contains ten questions. Each question is scored on a scale of 0-5. The scores for all questions answered are summed, then multiplied by two to obtain the index (range 0 to 100). Zero is equated with no disability and 100 is the maximum disability possible.

  2. Numeric Pain Rating Scale [1 minutes]

    The Numeric Pain Rating Scale (NPRS) that is a unidimensional measure of pain intensity in adults. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable".

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Volunteered to participate in the study.

  • Patients with 18-65 years

  • Low back pain for at least 3 months,

  • Reported pain severity of 2 or greater according to the numeric pain rating scale

Exclusion Criteria:
  • Previous spine or lower extremity surgery

  • Pregnancy

  • Severe hypermobility syndromes

  • Severe osteoporosis

  • Spondyloarthropathies

  • Spondylolisthesis

  • Systemic inflammatory diseases

  • Any neurological disorder that affects balance and gait

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kutahya Health Sciences University Evliya Celebi Hospital Physical Therapy and Rehabilitation Department Kutahya Turkey 43100

Sponsors and Collaborators

  • Kutahya Health Sciences University

Investigators

  • Principal Investigator: Ismail S [isaracoglu], P.hD., Kutahya Health Sciences University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ismail Saracoglu, Director, Kutahya Health Sciences University
ClinicalTrials.gov Identifier:
NCT05786118
Other Study ID Numbers:
  • CLBP and SIJ
First Posted:
Mar 27, 2023
Last Update Posted:
Mar 27, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2023