NCT04720846

Brief Summary

There is currently limited literature on a categorized physical therapy protocol for management of hip pain. Only a handful of studies have looked at the treatment of osteoarthritis of the hip with a standardized physical therapy treatment, primarily looking at manual therapy versus exercise therapy protocols. However, there are no studies observing the effect of a standardized physical therapy program on patients presenting with non-arthritic hip and groin pain. Based on the gap in the literature, this study will aim to assess the effect of matrix-based standard of care therapy in patients presenting with non-arthritic hip and groin pain.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
9mo left

Started Dec 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress88%
Dec 2020Feb 2027

Study Start

First participant enrolled

December 2, 2020

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 19, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 22, 2021

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2027

Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

6.2 years

First QC Date

January 19, 2021

Last Update Submit

April 23, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • iHOT-12 (International Hip Outcome Tool-12)

    iHOT-12 is used to assess quality of life in patients with hip disorders. Scores range from 0 to 100; a higher score represents a better quality of life.

    Up to 6 months

Secondary Outcomes (2)

  • NRS (numerical rating scale) pain

    Up to 6 months

  • Home exercise completion

    Up to 6 months

Study Arms (2)

Control

ACTIVE COMPARATOR

Patients will receive standard-of-care physical therapy.

Other: Standard-of-care physical therapy

Matrix-Based PT

EXPERIMENTAL

Patients will receive matrix-based physical therapy, in addition to standard-of-care physical therapy.

Other: Matrix-based physical therapyOther: Standard-of-care physical therapy

Interventions

Matrix-based physical therapy will be physical therapy that is based on the matrix categorization of the patient (stiff vs. mobile hips, weak vs. strong hips) and involves instructions on the amount of time that should be spent doing stretching and strengthening therapy.

Matrix-Based PT

Physical therapy that is being conducted as standard-of-care

ControlMatrix-Based PT

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • New patient presenting with non-arthritic hip impingement, hip pain, and groin pain (Tonnis 0-1)
  • years old

You may not qualify if:

  • Arthritic hip pain (Tonnis 2+)
  • \<18 and \>60 years old
  • History of spinal fusion surgery
  • History of low back pain with radicular pain
  • History of hip arthroscopy
  • History of inflammatory conditions, and other concurrent problems interfering with hip therapy (i.e., concurrent back/knee/foot/ankle/shoulder issues)
  • Patients currently taking TNF-alpha inhibitors for inflammatory conditions
  • History of prior knee osteotomy
  • Non-English speakers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hospital for Special Surgery

New York, New York, 10021, United States

RECRUITING

Study Officials

  • Peter Moley, MD

    Hospital for Special Surgery, New York

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jennifer Cheng

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 19, 2021

First Posted

January 22, 2021

Study Start

December 2, 2020

Primary Completion (Estimated)

February 1, 2027

Study Completion (Estimated)

February 1, 2027

Last Updated

April 28, 2026

Record last verified: 2026-04

Locations