Long-term Follow up of Patients With Longstanding Hip and Groin Pain

NCT ID: NCT03490071

Last Updated: 2023-03-16

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 81 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-01-01
• Study Completion Date: 2024-12-31

Brief Summary

In this longitudinal cohort study including young to middle aged people with longstanding hip and groin pain (LHGP) referred to tertiary care, we will collect data of patient reported symptoms, function and quality of life three and seven years after the initial contact with orthopedic surgeon.

Detailed Description

81 physically active patients (18-55 years) with (LHGP) who were enrolled in a cross-sectional study (Diagnosis and functional limitations in the young to middle-aged physically active population with long-standing hip/groin pain: A cross-sectional study) during the period October 2014 to January 2017 will be recruited to this longitudinal cohort study.

A research coordinator will contact the patients and provide them with written and oral information about the study. Patients who accept to participate will electronically complete the following questionnaires. The same questionnaires were included at baseline, i.e., in the cross-sectional study.

• Copenhagen Hip and Groin Outcome Score (HAGOS)
• HSAS - Hip Sports Activity Scale (HSAS)
• Patient Specific Functional Scale
• Medical Outcomes Study short form 36 (SF-36)
• K-10 questionnaire
• Self-Presentation in Exercise Questionnaire (SPEQ)
• Multidimensional Scale of Perceived Social Support (MSPSS)

Additional questions about treatment, medication, patient satisfaction and perceived change in hip function will be included.

For descriptive purposes, the mean difference (95% CI), or median (quartiles), between baseline and follow-up assessments will be used as appropriate. Separate linear regression models will be used to evaluate the change in each variable compared to baseline values.

Conditions

Hip Pain Chronic

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Unilateral or bilateral hip/groin pain >3 months
• Age 18-55 years
• No previous hip surgery

Exclusion Criteria

• Hip pathology (i.e., Perthes' disease)
• Verified moderate or severe osteoarthritis (OA) (Tönnis grade >1)
• Palpable hernia
• Low-back pain with a positive Lasègue test
• MRI-verified lower back/spine pathology (i.e., spinal stenosis, disc herniation)
• Other musculoskeletal co-morbidities overriding the hip-related symptoms and dysfunction
• Co-morbidities excluding physical activity and training
• Psycho-social disorders
• Drug abuse
• Not understanding the language of interest.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Lund University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Eva Ageberg, PhD

Role: PRINCIPAL_INVESTIGATOR

Lund University

Locations

Department of Health Sciences, Lund University

Lund, , Sweden

Site Status: RECRUITING

Countries

Sweden

Central Contacts

Eva Ageberg, PhD

Role: CONTACT

eva.ageberg@med.lu.se

+46 46 2224943

Anders Pålsson, PhD

Role: CONTACT

anders.palsson@med.lu.se

+46 733385393

Facility Contacts

Eva Ageberg, PhD

Role: primary

eva.ageberg@med.lu.se

+46 46 2224943

Other Identifiers

Lund LHGP

Identifier Type: -

Identifier Source: org_study_id