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Pelvic Stabilization Exercises & (PNF) on Pain, Disability & Functional Leg Length

R

Riphah International University

Status

Enrolling

Conditions

Anterior Innominate Iliosacral Dysfunction

Treatments

Other: Proprioceptive neuromuscular facilitation
Other: Pelvic stabilization exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT06108960
REC/RCR & AHS/23/0159

Details and patient eligibility

About

The aim of the study is to compare the effects of pelvic stabilization exercises and proprioceptive neuromuscular facilitation on pain, disability and functional leg length in patients with anterior innominate iliosacral dysfunction.

Full description

Illiosacral Dysfunction is accompanied by an abnormal movement of the ilium in relation to the sacrum, most commonly classified as either anterior or posterior innominate dysfunction. One of the unrecognized causes of low back and pelvic pain, as well as source of pain to proximal lower extremity is sacroiliac joint (SIJ) which arises from L5, S1 and in particular if there was an associated groin pain. There is a strong consensus on the effects of stabilization exercises in patients with chronic LBP, also some evidence for its benefits in patients with SJD. The aim of the study is to compare the effects of pelvic stabilization exercises and proprioceptive neuromuscular facilitation on pain, disability and functional leg length in patients with anterior innominate rotation dysfunction.

A total of 26 patients with Anterior innominate iliosacral dysfunction will be included in the study. Ethical approval will be taken from ethical committee of Riphah Internatinal University Lahore. Non-probability convenience sampling technique will be used to divide participants into group. Sample size is twenty-six. After taking informed consent and maintaining the confidentiality of individual participant, both groups will be treated with baseline treatment via the application of Hot pack. Group A will be treated with Proprioceptive neuromuscular facilitation and Group B will be treated with Pelvic Stabilization Exercises for eight weeks. Outcome measuring tools for pain (Numeric Pain Rating Scale), Functional Disability (Modified Oswestry low back pain disability Questionnaire) and Functional Leg length (Tape Method) will be noted pre, 4th week and post treatment. Data will be Analyzed by SPSS version 29. Descriptive statistics will be used for demographics. The normality of the data will be assessed by Shapiro-Wilk test. If the data is normally distributed parametric test i.e., T-Test will be used for inter group difference while Paired Sample T-Test will be used for intra group pre and post treatment difference. If the data is not normally distributed a nonparametric test i.e., Mann-Whitney test will be used.

Enrollment

26 estimated patients

Sex

All

Ages

25 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient within ages of 25 and 45 years.
  • Both male and female participants will be included.
  • Episode of Lumbopelvic pain within the previous 6 weeks with pain radiating till the knee and associated groin pain.
  • Pain and tenderness at SIJ
  • The diagnostic criteria for SJD were five clinical tests Compression, Distraction, sacral thrust, thigh thrust and Gaenslen test (patient with a minimum of 3 positive results among the 5 provocation tests)
  • Positive Special test for Anterior Innominate Dysfunction (Standing flexion test, Seated flexion test, Supine to sit test and Gillet test)
  • NPRS = 3 to 6

Exclusion criteria

  • Any other medical/systemic illness relevant to lower back and lower extremity
  • Previous major surgery for lower back and lower extremity
  • SLR Less than 45°
  • Pain radiating past the knee
  • Pregnant and lactating females
  • Had been diagnosed by physician with a diagnosis other than SIJD
  • Receiving manual therapy for the sacroiliac joint in the past 3 month

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

26 participants in 2 patient groups

Proprioceptive neuromuscular facilitation
Experimental group
Description:
The patients will be positioned in supine lying and then contract relax will be performed on affected side of pelvis first in D1 pattern (anterior elevation and posterior depression) 3 times with 10 sec contractions and 5 sec relaxations in 1 set. Then in D2 pattern (posterior elevation and anterior depression) 3 times with 10 sec contractions and 5 sec relaxations in 1 set. 3 set of each diagonal pattern to be performed in 1 treatment session alternatively. Treatment will be given for a period of 4 days a week for 8 weeks
Treatment:
Other: Proprioceptive neuromuscular facilitation
Pelvic stabilization exercises
Experimental group
Description:
All participants will receive training programs for the eight levels of training from static to dynamic conditions. The practiced therapy method will first taught by a physical therapist with a verbal explanation and visual aids (such as photographs) in each group. The therapist will supervise all stages of the exercise therapy to ensure the patients correctly performed the exercises. The supervised exercise intervention will be conducted 3 days a week for 8 weeks.
Treatment:
Other: Pelvic stabilization exercises

Trial contacts and locations

1

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Central trial contact

Imran Amjad, PHD

Data sourced from clinicaltrials.gov

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