Effects of Functional Motor Control on Pain, Flexibility, Lower Extremity Function With ITBS

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06131658
Collaborator
(none)
18
1
2
4
4.5

Study Details

Study Description

Brief Summary

The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A & B through sealed envelope method by non-probability convenient random sampling technique. Subjects in group A will receive functional motor control exercises. Group B will receive conventional exercises.

Condition or Disease Intervention/Treatment Phase
  • Other: Functional motor control excercise
  • Other: convectional excercise
N/A

Detailed Description

The objective of this study is to determine the effects of functional motor control exercises on pain, flexibility and lower limb functional. It will be randomized controlled trial (RCT) research design at Pakistan sports board through non probability convenience sampling technique on 18 runners' athletes which will be allocated using random sampling through computerized generated number into Group A and Group B, 9 athletes will be in each group. Group A (interventional) will be given conventional training with functional motor exercise and Group B (control) will be given conventional training. There will be 3 sessions in a week for 6 weeks. The baseline scoring will be on 1st day, follow up will be taken at 6th week. Assessment will be made by Numeric pain rating scale, Lower extremity functional scale (LEFS), dynamometer, Single leg mini squat, Y balance. Data will be analyzed during SPSS software version 26. After assessing normality of data by Shapiro-Wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two group

Study Design

Study Type:
Interventional
Anticipated Enrollment :
18 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized clinical trialRandomized clinical trial
Masking:
Single (Outcomes Assessor)
Masking Description:
assessor who will take reading is blind
Primary Purpose:
Other
Official Title:
Effects of Functional Motor Control Exercise on Pain, Flexibility, Lower Extremity Function Among Runners With Iliotibial Band Syndrome
Actual Study Start Date :
Oct 20, 2023
Anticipated Primary Completion Date :
Feb 20, 2024
Anticipated Study Completion Date :
Feb 20, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Functional motor control excercise

Functional motor control exercise Includes side plank with clamshell, Side plank with hip abduction, Side-lying hip abduction, Lateral monster walk, Hip hikes, Single leg squat, TKE with T-band-hip abduction All exercises done with 2 sets of 10 reps with 3 sessions per week for 6 weeks

Other: Functional motor control excercise
This include functional motor control thrice a week for six weeks

Experimental: conventional exercise

The conventional exercise included 4 stages of self-myofascial techniques, strengthening, and integration techniques. In the first phase, individuals did fascial release exercises using foam rolls, focusing on tensor fascia latae, iliotibial band, and hip adductor muscles, and tennis balls for the quadratus lumborum. The exercises were performed at high-intensity maximum pain tolerance for 30 seconds or low-intensity minimum pain tolerance for 90 seconds.

Other: convectional excercise
This include convectional exercise thrice a week for six weeks

Outcome Measures

Primary Outcome Measures

  1. pain measurement [pre and 6 weeks post interventional]

    pain will be assess by Numeric pain rating scale

  2. flexibility [pre and 6 weeks post interventional]

    flexibility will be assess by dynamometer, Y balance

  3. lower extremity function [pre and 6 weeks post interventional]

    lower extremity function will be assess by lower limb extremity scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • male and female athlete within 19-40 years,

  • running a minimum average of 15 running kilometers,

  • Runners with one sided iliotibial band syndrome for at least 3 months were included,

  • Pain along IT band at either Gerdy's tubercle or the lateral femoral epicondyle during running,

  • positive stiffness with Ober's test, and

  • reporting pain during Noble's compression test.

Exclusion Criteria:
  • Individuals with a history of previous knee trauma of past 6 months,

  • Individuals with a history of previous knee surgery of past 6 months,

  • Other knee abnormalities including patellofemoral joint pain,

  • popliteus tendinitis,

  • lateral meniscal injury,

  • Degenerative joint disease, and

  • lateral collateral ligament sprain to the affected side.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jawad Club Faisalābad Punjab Pakistan 37700

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: maham Athar, DPT, Investigator

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT06131658
Other Study ID Numbers:
  • REC/RCR&AHS/23/0429
First Posted:
Nov 14, 2023
Last Update Posted:
Nov 14, 2023
Last Verified:
Nov 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
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 14, 2023