NCT06841588

Brief Summary

This study aims to highlight and investigate the effectiveness of two common management practices in physiotherapy, dry needling intervention as a soft tissue technique and Mulligan mobilization with movements MWM as a joint technique, on pain, function, and range of motion among athletes with hip adductor-related groin pain and dysfunction.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2020

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

May 1, 2020

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2021

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 17, 2021

Completed
3.4 years until next milestone

First Submitted

Initial submission to the registry

January 20, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
Last Updated

February 24, 2025

Status Verified

June 1, 2023

Enrollment Period

11 months

First QC Date

January 20, 2025

Last Update Submit

February 18, 2025

Conditions

Keywords

Athleteship adductorgroin painathletes with groin painathletes with hip dysfunction

Outcome Measures

Primary Outcomes (5)

  • Sheet of Demographic Data

    Demographic, personal data, and injury history were obtained at baseline from the patient interview and recorded on a data collection sheet

    pre and 1 day post treatment

  • Numeric Pain Rating Scale NPRS

    The Numeric Pain Rating Scale (NPRS) is valid and reliable, a self-assessing questionnaire , used to assess the severity of pain. 0- 10 scale where 0 represents "no pain" and 10 representing "unbearable pain." Each participant was asked to indicate the pain level before and after treatment.

    pre and 1 day post treatment

  • Y-Balance Test YBT

    The Y balance test was developed from the star excursion balance test (SEBT) and assesses performance during single-leg balance with reaching in the 3 directions: anterior, posteromedial, and posterolateral. the patient stands on one leg while reaching out in 3 different directions with the other lower extremity.

    pre and 1 day post treatment

  • FABER Test

    To assess the adductor muscle tightness and shortening due to injury. FABER test is used as a provocation special test but has also been used as a measurement of combined hip range of motion, also useful tools for the hip examination, particularly for anterior hip or groin pain. The patient lies supine on the examination table. The hip and knee of the tested leg are flexed, abducted, and externally rotated, as the foot of the tested leg is placed on the contralateral thigh just proximal to the knee. While stabilizing the pelvis on the contralateral side, gentle pressure is applied downwards on the knee of the tested leg, also measuring the distance from the lateral condyle of the knee to the surface of the examination table for both affected and none affected knees.

    pre and 1 day post treatment

  • Five Seconds Copenhagen Squeeze Test

    The therapist placed his arms between the athlete's knees and asked the athlete to squeeze the legs as hard as possible for five seconds, then, scored any pain in the groin area on a scale of 0 to 10 NPRS Scale

    pre and 1 day post treatment

Study Arms (2)

Mulligan's Mobilization with Movement and Dry Needling

ACTIVE COMPARATOR

the intervention group 1 was treated using Mulligan Mobilization with Movements and Dry Needling (DN\&MWM) for soft tissue trigger points, (N=15).

Other: Mulligan's Mobilization with Movement and Dry Needling

Dry Needling

ACTIVE COMPARATOR

the intervention group 2 was treated using Dry Needling (DN) for soft tissue trigger points, (N=15).

Other: Dry Needling (DN)

Interventions

the intervention group 1 was treated using Mulligan Mobilization with Movements and Dry Needling (DN\&MWM) for soft tissue trigger points, (N=15). The treatment duration was 6 sessions, 3 sessions per week ( day after day).

Mulligan's Mobilization with Movement and Dry Needling

The intervention group 2 was treated using Dry Needling (DN) for soft tissue trigger points, (N=15). The treatment duration was 6 sessions, 3 sessions per week ( day after day).

Dry Needling

Eligibility Criteria

Age15 Years - 35 Years
Sexmale(Gender-based eligibility)
Gender Eligibility DetailsAthletes males
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Athletes suffered from unilateral adductor-related groin pain, grades 1 and 2.
  • Acute, subacute, or chronic athletes with hip adductor-related groin pain and dysfunction.
  • Groin pain during or after activities.
  • Pain at palpation of the adductors and their origin.
  • Pain on resistance against adduction.
  • Aged 15- 35 years old.

You may not qualify if:

  • Patients with other causes of groin pain such as:
  • Lymphadenitis.
  • Prostatitis, Urinary infections, Malignancy.
  • Spinal pathology.
  • Hip joint osteoarthritis.
  • Inguinal-related or Iliopsoas-related groin pain.
  • Femoral or Inguinal hernia.
  • Referral pain and adductor strain grade 3.
  • Current use of medication.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ayman Daragmah

Ramallah, P125, Palestinian Territories

Location

MeSH Terms

Interventions

MovementDry Needling

Intervention Hierarchy (Ancestors)

Physiological PhenomenaMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaComplementary TherapiesTherapeuticsPhysical Therapy Modalities

Study Officials

  • Daragmah, Master degree

    Al-Quds University

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

January 20, 2025

First Posted

February 24, 2025

Study Start

May 1, 2020

Primary Completion

March 15, 2021

Study Completion

August 17, 2021

Last Updated

February 24, 2025

Record last verified: 2023-06

Data Sharing

IPD Sharing
Will not share

Locations