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Effectiveness of Core Stabilization Exercises in Rotator Cuff Injuries

A

Ahi Evran University Education and Research Hospital

Status

Begins enrollment this month

Conditions

Core Exercises Training
Rotator Cuff Injury (RCI)

Treatments

Other: Classic Trunk and Abdominal Strengthening Program
Other: Conventional Rehabilitation
Other: Core Stabilization Exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT07377292
AhievranUERH-FTR-SD-01

Details and patient eligibility

About

The aim of this study is to investigate the effectiveness of core stabilization exercises added to conventional physical therapy in patients aged 40-60 with rotator cuff tears, compared to classic trunk and abdominal muscle strengthening exercises.

Full description

Rotator cuff tears are classified as full-thickness and partial tears. Partial tears are a clinical condition commonly seen in the early stages but can often be treated with conservative methods. Partial tears can develop as a result of repetitive microtraumas, postural abnormalities, muscle imbalances, and deficiencies in the biomechanical chain. This condition affects not only the local shoulder muscles but also the scapulothoracic rhythm and trunk control. Recent studies have shown that shoulder function is closely related not only to local muscle strength but also to the integrity of the kinetic chain. The trunk (core) muscles are particularly critical for maintaining posture, transferring force during upper extremity movements, and stabilizing the distal segments. Inadequate trunk stabilization can lead to increased loads on the shoulder joint and elevated stress on the rotator cuff. Therefore, the aim of this thesis study is to examine the effectiveness of core stabilization exercises applied to individuals diagnosed with rotator cuff partial tears on pain, shoulder function, and clinical recovery, and to contribute scientifically to conservative rehabilitation approaches.

Enrollment

69 estimated patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 40 to 60 years with a partial supraspinatus tear detected by MRI, reported by a radiologist, and confirmed by a physiatrist.
  • Patients who test positive for at least two of the Jobe, Hawkins and Neer tests during the physical examination
  • Patients with a visual analog scale (VAS) score between 3.5 and 7.4 millimeters (mm)

Exclusion criteria

  • Participants do not wish to continue treatment for any reason
  • Complete or massive rotator cuff tear
  • Use of non-steroidal or steroidal anti-inflammatory drugs
  • If they have received shoulder injections or physical therapy within the three months prior to the study
  • History of acute trauma
  • Presence of neurological disease
  • History of surgery on the treated shoulder
  • Symptomatic acromioclavicular joint arthritis
  • Frozen shoulder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

69 participants in 3 patient groups, including a placebo group

Core Stabilization Group
Active Comparator group
Description:
Patients received conventional rehabilitation for the affected shoulder 5 days a week for 4 weeks and core stabilization exercises 3 days a week for 4 weeks.
Treatment:
Other: Core Stabilization Exercises
Other: Conventional Rehabilitation
Classic Body Exercise Group
Active Comparator group
Description:
Patients will receive conventional rehabilitation for the affected shoulder 5 days a week for 4 weeks, along with a classic trunk and abdominal strengthening program 3 days a week for 4 weeks.
Treatment:
Other: Conventional Rehabilitation
Other: Classic Trunk and Abdominal Strengthening Program
Control Group
Placebo Comparator group
Description:
Patients will receive conventional rehabilitation for the affected shoulder five days a week for four weeks.
Treatment:
Other: Conventional Rehabilitation

Trial contacts and locations

1

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Central trial contact

Başak ÇİĞDEM KARAÇAY; Süleyman DALAR

Data sourced from clinicaltrials.gov

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