Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07597343

The 'As Soon As Possible (ASAP)' Intervention for Enhancing Therapeutic Exercise Adherence Among Patients With Greater Trochanteric Pain Syndrome (GTPS): A Feasibility Trial

Led by Loughborough University · Updated on 2026-05-19

60

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

Sponsors

L

Loughborough University

Lead Sponsor

U

University Hospitals, Leicester

Collaborating Sponsor

AI-Summary

What this Trial Is About

Greater Trochanteric Pain Syndrome (GTPS) is a condition causing pain on the outer side of the hip, often affecting middle-aged women. This trial evaluates a simple exercise timing approach to see if following a prescribed hip exercise programme early in the day helps improve adherence. Researchers compare whether timing guidance, with or without reminders, is easier and more acceptable than usual care for adults diagnosed with GTPS. Participants are randomly assigned to one of three groups: one group receives information about exercising early in the morning plus weekly digital reminders; another group receives only the information without reminders; and the third group follows their usual prescribed exercises without any timing guidance or reminders. All participants follow the same hip-strengthening exercises prescribed by their healthcare provider over a 28-day intervention period. During the study, participants complete a short daily survey about their exercise for 28 days and fill out online questionnaires on hip pain, movement, and exercise at five points over about three months. Some participants will join online group discussions at the end to share their experiences. Researchers monitor recruitment, retention, questionnaire completion, and participant feedback to assess the feasibility of this approach and inform future larger trials.

CONDITIONS

Brief Title

Enhancing Exercise Adherence Among Patients With Lateral Hip Pain

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Greater Trochanteric Pain Syndrome (GTPS) by a qualified healthcare provider
  • Aged 18 years or older
  • Willingness to participate in the study
  • Ability to understand and provide informed consent
  • Physically able to safely perform prescribed exercises as assessed by NHS healthcare practitioner
  • Own a mobile phone
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Severe medical or psychiatric conditions affecting ability to participate or comply with the exercise program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) at the Sport and Exercise Medicine clinic for eligibility assessment and enrollment

Treatment

Duration - 28 days

Participants follow a prescribed hip-strengthening exercise programme as part of standard clinical care. Depending on group assignment, participants receive guidance on completing exercises early in the morning, with or without weekly digital reminders, or continue usual care without timing guidance.

Daily online adherence surveys completed by participants for 28 days; study conducted entirely online after enrollment

Follow-up

Duration - Up to 12 weeks from baseline (Day 1 to Day 84)

Participants complete outcome assessments online to monitor adherence and symptom response after the active intervention period.

Online assessments at Day 14, Day 28, Day 42, and Day 84

Trial Site Locations

Total: 1 location

1

University Hospitals of Leicester NHT Trust, Department of Musculoskeletal, Sport & Exercise Medicine

Leicester, Leictershaire, United Kingdom, LE5 4PW

Actively Recruiting

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Research Team

W

Wafa R Alrubaia, MSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

3

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