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Feasibility of Home Exercises With the Addition of a Corticosteroid Injection in Patients With Lateral Hip Pain in General Practice

Primary Purpose

Lateral Hip Pain, Gluteal Tendinopathy, Greater Trochanteric Pain Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Exercises and CSI
Sponsored by
Aalborg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Lateral Hip Pain

Eligibility Criteria

35 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • >35 years of age
  • Self-reported pain on the outside of the hip for at least 12 weeks with an average intensity of present pain over the last week of at least 4/10 on a numeric rating scale 0-10 (0 being no hip pain and 10 being worst hip pain imaginable)
  • Access to a computer, smartphone or tablet with internet connection
  • Tenderness on palpation of the greater trochanter
  • Reproduction of lateral hip pain with 30 sec single leg stance test
  • Ability to speak and understand Danish (written and oral)
  • In case of bilateral hip pain, the study hip will be the most painful at inclusion

Exclusion Criteria:

  • Corticosteroid injection in the affected hip or other new treatment by a health professional within the last 3 months
  • History of systemic inflammatory diseases, e.g. rheumatoid arthritis, spondyloarthritis
  • Weekly intake of oral glucocorticoids
  • History of other hip conditions, e.g. clinically significant hip osteoarthritis, hip dysplasia, prior hip surgery
  • History of prior lumbar back surgery
  • Current low back pain or episodes of low back pain within the last 3 months that have caused sick leave and/or treatment by a health professional
  • Physical or mental disabilities that make it impossible to understand and/or perform exercises and complete questionnaires
  • Current or planned pregnancy or breastfeeding

Sites / Locations

  • Center for General Practice at Aalborg UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Exercises and CSI

Arm Description

A corticosteroid injection in the lateral hip prior to performing an 8-week home exercise program

Outcomes

Primary Outcome Measures

Acceptability of performing our exercise program
7-point Likert scale range "very unacceptable" to "very acceptable"
Acceptability of performing exercises after receiving a corticosteroid injection
7-point Likert scale range "very unacceptable" to "very acceptable"

Secondary Outcome Measures

Global Rating of Change
This is determined by asking the question "How is your lateral hip pain now compared to when you first came in for treatment in this project?", which will be responded to with a 7-point Likert scale ranging from "very much worse" to "very much better".
Patent Acceptable Symptom State
This will be identified by asking the patient to answer yes or no to the question "Is your lateral hip pain at an acceptable level that does not require any further treatment?"
Pain Self-Efficacy Questionnaire
This is a self-reported measure used to assess how confident patients are in performing activities while in pain. The outcome is a score of 0 to 60, with higher score indicating higher self-efficacy. We will use a Danish validated version
Health-related quality of life
We will use EuroQol-5D-5L. This is a standardized instrument to assess health related quality of life.
Compliance to exercises
Participants will record their exercise sessions using an exercise diary

Full Information

First Posted
September 14, 2021
Last Updated
October 8, 2021
Sponsor
Aalborg University
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1. Study Identification

Unique Protocol Identification Number
NCT05086926
Brief Title
Feasibility of Home Exercises With the Addition of a Corticosteroid Injection in Patients With Lateral Hip Pain in General Practice
Official Title
Feasibility of a Home Exercise Program With the Addition of a Corticosteroid Injection in Patients With Greater Trochanteric Pain Syndrome in General Practice
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 2021 (Anticipated)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
February 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aalborg University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Pain on the lateral side of the hip is a common condition in general practice, however there is limited evidence on how to best manage the condition. The purpose of this study is to evaluate the feasibility of a combined treatment before comparing this treatment in a larger clinical trial. For the present study 20 patients with lateral hip pain will be invited to receive a corticosteroid injection in the lateral hip prior to performing our exercise program for 8 weeks. After 4 weeks we will do a short interview to get feedback on the exercise program. After 8 weeks we will evaluate the acceptability of the combined treament.
Detailed Description
BACKGROUND: Lateral hip pain or greater trochanteric pain syndrome (GTPS) is pain on the outside of the hip due to tendon pathology of the hip abductor tendons. The incidence in primary care has been reported to be 1.6-3.3 per 1000 patients per year. At present, there is no evidence-based guidelines for the treatment of GTPS in primary care. The investigators of the present study have developed an exercise protocol that is planned be evaluated in a future randomized controlled trial in combination with a corticosteroid injection. OBJECTIVE: The purpose of this study is to evaluate feasibility of a home exercise program with the addition of a corticosteroid injection in patients with GTPS in general practice. The primary aim is to evaluate patient acceptability of 1) performing our exercise program 2) performing exercises after receiving a corticosteroid injection. The secondary aim is to obtain feedback from patients through qualitative interviews to be able to refine the exercise intervention after the study is completed. If the combined treatment is found feasible, it is planned to evaluate the effect in a large randomized controlled trial in the future. STUDY DESIGN: The study design is a mixed methods feasibility study. The participants are patients with GTPS that will receive a combined treatment of one corticosteroid injection in the lateral hip and a home exercise program, which is to be performed for a period of eight weeks. The acceptability of the combined intervention will be evaluated after 8 weeks. RECRUITMENT OF PARTICIPANTS: Patients with GTPS will be recruited from general practice and a private rheumatology practice. Patients will be considered for inclusion if they present to their practitioner with self-reported lateral hip pain. The project manager will make a screening of eligibility by telephone. Those not excluded based on this screening, will be invited to a clinical examination where final eligibility is determined. ENDPOINTS: Baseline is at the clinical examination. One week from baseline there will be a short phone contact to the participants in order to clarify any questions related to the exercise program. No data will be obtained at this point. At 4 weeks there will be a phone interview which also serves as a booster session where the participants are encouraged to maintain their exercise routine. At 8 weeks there will be a physical visit where the participants will hand in their exercise diaries and complete the final questionnaires. CRITERIA OF FEASIBILITY: To conclude that the combined treatments are feasible, ≥ 75% of patients must rate the treatment as 'acceptable'. If any participant drops out after the injection, they will be dichotomized as "not acceptable". A minimum of 15/20 training diaries must be handed in at 8-weeks follow-up. Based on the returned training diaries, ≥ 75% of participants need to complete ≥ 20/28 possible training sessions. A training session will be considered completed if the participant has performed at least one set of each exercise. In case the combined treatments do not prove feasible according to this set of criteria, it is planned to refine the intervention based on feedback from the interviews and evaluate with a small group of patients for a shorter period of time.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lateral Hip Pain, Gluteal Tendinopathy, Greater Trochanteric Pain Syndrome

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exercises and CSI
Arm Type
Experimental
Arm Description
A corticosteroid injection in the lateral hip prior to performing an 8-week home exercise program
Intervention Type
Combination Product
Intervention Name(s)
Exercises and CSI
Intervention Description
Corticosteroid injection: The project manager will give the participants one injection with cortisone and lidocaine in the lateral hip at baseline. The procedure will be performed aseptically. Home exercise program: The exercise programis based on previous literature and expert opinions that has been synthesized in a Delphi study conducted by our research group. The exercise program consists of three body weighted strength exercises, that are to be performed every second day for a period of 8 weeks. Exercise instructions will be available as a handout and online with video instructions. The corticosteroid injection usually causes a flare-up in pain with a duration of up to 48 hours. Participants will be instructed to begin the exercises as soon as possible after this flare-up has settled.
Primary Outcome Measure Information:
Title
Acceptability of performing our exercise program
Description
7-point Likert scale range "very unacceptable" to "very acceptable"
Time Frame
8 weeks
Title
Acceptability of performing exercises after receiving a corticosteroid injection
Description
7-point Likert scale range "very unacceptable" to "very acceptable"
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Global Rating of Change
Description
This is determined by asking the question "How is your lateral hip pain now compared to when you first came in for treatment in this project?", which will be responded to with a 7-point Likert scale ranging from "very much worse" to "very much better".
Time Frame
4 and 8 weeks
Title
Patent Acceptable Symptom State
Description
This will be identified by asking the patient to answer yes or no to the question "Is your lateral hip pain at an acceptable level that does not require any further treatment?"
Time Frame
4 and 8 weeks
Title
Pain Self-Efficacy Questionnaire
Description
This is a self-reported measure used to assess how confident patients are in performing activities while in pain. The outcome is a score of 0 to 60, with higher score indicating higher self-efficacy. We will use a Danish validated version
Time Frame
4 and 8 weeks
Title
Health-related quality of life
Description
We will use EuroQol-5D-5L. This is a standardized instrument to assess health related quality of life.
Time Frame
4 and 8 weeks
Title
Compliance to exercises
Description
Participants will record their exercise sessions using an exercise diary
Time Frame
8 weeks
Other Pre-specified Outcome Measures:
Title
Qualitative outcomes
Description
Short interview to obtain qualitative feedback from participants. Questions: How was your experience in general with completing this exercise program? Which challenges did you experience? How did you find the difficulty of the levels in the exercise program? Did you have any challenges with the training diary? Did you find the phone call from the project manager at one week useful?
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >35 years of age Self-reported pain on the outside of the hip for at least 12 weeks with an average intensity of present pain over the last week of at least 4/10 on a numeric rating scale 0-10 (0 being no hip pain and 10 being worst hip pain imaginable) Access to a computer, smartphone or tablet with internet connection Tenderness on palpation of the greater trochanter Reproduction of lateral hip pain with 30 sec single leg stance test Ability to speak and understand Danish (written and oral) In case of bilateral hip pain, the study hip will be the most painful at inclusion Exclusion Criteria: Corticosteroid injection in the affected hip or other new treatment by a health professional within the last 3 months History of systemic inflammatory diseases, e.g. rheumatoid arthritis, spondyloarthritis Weekly intake of oral glucocorticoids History of other hip conditions, e.g. clinically significant hip osteoarthritis, hip dysplasia, prior hip surgery History of prior lumbar back surgery Current low back pain or episodes of low back pain within the last 3 months that have caused sick leave and/or treatment by a health professional Physical or mental disabilities that make it impossible to understand and/or perform exercises and complete questionnaires Current or planned pregnancy or breastfeeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sabina Vistrup, MD
Phone
40125067
Email
sabinavistrup@dcm.aau.dk
Facility Information:
Facility Name
Center for General Practice at Aalborg University
City
Aalborg
ZIP/Postal Code
9220
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sabina Vistrup
Phone
40125067
Email
sabinavistrup@dcm.aau.dk

12. IPD Sharing Statement

Plan to Share IPD
No

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Feasibility of Home Exercises With the Addition of a Corticosteroid Injection in Patients With Lateral Hip Pain in General Practice

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