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Conservative Management of Femoroacetabular Impingement

H

High Point University

Status

Completed

Conditions

Femoroacetabular Impingement

Treatments

Other: Manual therapy plus exercise
Other: Advice and home exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT01814124
201207-116

Details and patient eligibility

About

Femoroacetabular impingement (FAI) is recognized as a formal source of hip pain and disability typically affecting the young adult, active population and has been identified as a precursor to hip osteoarthritis (OA). Common impairments include sharp, anterior groin pain in a position of hip flexion limiting patients' ability to tolerate prolonged sitting, squatting, stair climbing, etc. resulting in both work limitations and decreased social participation. Manual therapy and exercise is known to be effective in reducing pain and increasing physical function in the management of hip OA. To the extent that FAI is often a precursor to developing hip OA, logic would seem to dictate a manual therapy plus exercise approach to decrease pain and disability and potentially prevent or delay osteoarthritis related surgery. Currently, surgery is considered the first line of treatment with respect to FAI. However, there is a lack of evidence to support or refute the use of conservative treatment interventions in this patient population.

This study is designed to investigate the benefits of physical therapy interventions (manual therapy and exercise) over usual care for improving pain and physical function in patients with FAI of the hip. For this study, 52 participants will be recruited from the Department of Orthopaedic Surgery, Wake Forest Baptist Medical Center, for an outpatient consultation for consideration of hip arthroscopy surgery. Participants will include those patients who meet clinical and radiological criteria for formal diagnosis of FAI. Participants will be randomized into two treatment groups. Participants in one group will receive usual care plus manual therapy directed at the hip as well as a supervised exercise program and home exercise program twice weekly for six weeks. Participants in the usual care group will receive usual care as prescribed by the physician. Changes in pain, physical function and benefits of the intervention will be assessed over six weeks. Should this research study demonstrate treatment effectiveness of physical therapy intervention in patients diagnosed with FAI of the hip, manual therapy plus exercise may have the potential to delay or prevent surgery in this patient population. Further, to the extent to which FAI has been shown to lead to later development of hip OA, effective treatment interventions may help to delay or prevent secondary osteoarthritis related changes as well as total joint replacement surgery associated with hip OA. This study will provide preliminary data that can be used to prepare further grant applications designed to determine the safest, most effective treatments for patients with FAI.

Enrollment

18 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The participants will include new and existing patients with a diagnosis of femoroacetabular impingement and are being seen for an outpatient consultation for consideration of hip arthroscopy surgery.
  • From direct correspondence with Dr. Stubbs, criteria for formal diagnosis of FAI includes a combination of clinical diagnosis supported with radiography.
  • Clinical examination typically consists of reported hip pain, decreased flexion (<95o), decreased internal rotation (<10o), and
  • a positive anterior impingement test result (report of deep, anterior groin pain following combination of flexion, internal rotation, and adduction).
  • Use of an alpha angle is also used as a distinct characteristic with patient's having an alpha angle of > 50-55 degrees at increased risk for FAI.

Exclusion criteria

  • previous hip surgery;
  • any other surgical procedure of the lower limbs in the prior 6 months;
  • pre-existing disease state of the hip such as rheumatoid arthritis;
  • fracture;
  • congenital/developmental hip dysplasia;
  • initiation of opioid analgesia or cortico-steroid or analgesic injection intervention for hip pain within prior 30 days;
  • physical impairments unrelated to the hip preventing safe participation in exercise, manual therapy, walking or stationary cycling;
  • advanced osteoporosis;
  • body mass index > 38;
  • significant cardio-pulmonary disease;
  • cardiac pacemaker;
  • stated inability to complete the proposed course of intervention and follow-up;
  • insufficient English language skills to comprehend assessment tools;
  • resident greater than 90 minutes from Wake Forest Baptist Medical Center.
  • Individuals with contraindications to treatment with mobilization and manipulation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

18 participants in 2 patient groups

Advice and home exercise
Active Comparator group
Description:
All participants will be given a handout consisting of education about avoidance of certain activities as well as 3 stretches and 3 strengthening exercises to be performed as a home exercise program 2-3x/week
Treatment:
Other: Advice and home exercise
Manual Therapy Plus Exercise
Experimental group
Description:
Participants in this group will be given the same handout consisting of education about avoidance of certain activities as well as 3 stretches and 3 strengthening exercises to be performed as a home exercise program 2-3x/week. Participants in this group will also receive 12 individualized physical therapy treatment sessions (2x/week for 6 weeks) consisting of both manual therapy and exercise directed at the hip and surrounding areas based upon findings from the initial examination. Participants will also be given additional exercises to be performed at home as directed by the treating physical therapist
Treatment:
Other: Manual therapy plus exercise
Other: Advice and home exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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