Proprioceptive Training vs. Hip Abductor With External Rotator Strengthening in Patients With Patellofemoral Pain

Sponsor
King Saud University (Other)
Overall Status
Completed
CT.gov ID
NCT05698797
Collaborator
(none)
45
1
3
7.4
6.1

Study Details

Study Description

Brief Summary

Patellofemoral pain syndrome (PFPS) is a common musculoskeletal disorder characterized by an insidious onset of pain in the knee's anterior /retro-patellar / peripatellar region. Even though various rehabilitation approaches, including hip strengthening and proprioceptive training, are being considered for managing PFPS, the most appropriate treatment from these two is still unclear. Therefore, this study aimed to compare the program consisting of hip abductors and external rotators strengthening exercises vs. the program consisting of proprioceptive training of the knee to identify the most effective rehabilitation approach for patients suffering from PFPS.

Condition or Disease Intervention/Treatment Phase
  • Other: Hip strengthening exercises
  • Other: Proprioceptive training
  • Other: Conventional physical therapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
45 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Proprioceptive Training vs. Hip Abductor With External Rotator Strengthening on Pain and Functions in Patients With Patellofemoral Pain Syndrome
Actual Study Start Date :
Nov 11, 2021
Actual Primary Completion Date :
May 6, 2022
Actual Study Completion Date :
Jun 24, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group 1

In this group participants received hip abductor and external rotator strengthening exercises in addition to conventional physical therapy.

Other: Hip strengthening exercises
Hip abductor and external rotator strengthening exercises were performed for 4 weeks.

Active Comparator: Experimental group 2

In this group participants received proprioceptive training and conventional physical therapy.

Other: Proprioceptive training
Proprioceptive training consisted of eight exercises was performed for 4 weeks.

Active Comparator: Control group

In this group participants received conventional physical therapy alone.

Other: Conventional physical therapy
Conventional physical therapy included interferential therapy and two types of knee-strengthening exercises.

Outcome Measures

Primary Outcome Measures

  1. Kujala Anterior Knee Pain Scale (AKPS) [4 weeks.]

    Pain was measured using the AKPS. The AKPS is scored from a minimum score of 0 to a maximum score of 100 points. Lower scores indicate greater pain and disability.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-35 years

  • Patients diagnosed recently by an orthopedic surgeon for Patello-femoral pain syndrome

  • experiencing anterior/retro patellar knee pain during activities,

  • insidious onset of symptoms not linked to trauma,

  • pain persisting for no less than four weeks,

  • pain on palpation of the patellar facets,

  • pain when stepping down from a 25-cm step or during a double-legged squat.

Exclusion Criteria:
  • Patients with recent lower limb fractures or dislocations,

  • knee/hip joint surgery,

  • signs, symptoms, or radiological findings of intra-articular pathology such as effusion, ligamentous or meniscal involvement,

  • those with indications of patellar apprehension,

  • referred pain from the hip, back, or sacroiliac joint,

  • acute knee strain or sprain,

  • on medication such as NSAIDs or corticosteroids,

  • degenerative and infectious arthritis

Contacts and Locations

Locations

Site City State Country Postal Code
1 King Saud University Riyadh Saudi Arabia 11433

Sponsors and Collaborators

  • King Saud University

Investigators

  • Principal Investigator: Masood Khan, M.P.Th, King Saud University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Masood Khan, Principal Investigator, King Saud University
ClinicalTrials.gov Identifier:
NCT05698797
Other Study ID Numbers:
  • AWH/EC/03/2021
First Posted:
Jan 26, 2023
Last Update Posted:
Jan 26, 2023
Last Verified:
Jan 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 Masood Khan, Principal Investigator, King Saud University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 26, 2023