"Effectiveness of a Telerehabilitation Program Versus a Conventional Rehabilitation Program in Patients With Subacromial Pain"

Starting soon · Not applicable

Conditions studied: Subacromial Impingement Syndrome

In brief

The purpose of this prospective, randomized, parallel-group, single-center, controlled non-inferiority clinical trial is to determine whether a telerehabilitation program is non-inferior to a conventional rehabilitation program in patients with subacromial pain. Subacromial pain is a prevalent musculoskeletal condition, and while therapeutic exercise is the cornerstone of conservative management, adherence to home programs is often low. Conversely, conventional in-person physical therapy presents logistical and economic barriers for patients. This study aims to evaluate if a well-designed telerehabilitation program, utilizing information and communication technologies for remote monitoring, can provide an effective, accessible, and non-inferior alternative to conventional care. The primary outcome measured will be the change in shoulder function utilizing the QuickDASH questionnaire at 12 weeks. Secondary outcomes will assess pain intensity (VAS), range of motion (ROM), treatment adherence, and long-term functional outcomes.

Key facts

Study ID

NCT07536009

Run by

Instituto Mexicano del Seguro Social

People needed

82

Starts

2026-04-15

Expected to finish

2027-05-30

Last updated by the study team

2026-04-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Men and women aged 18 years or older.
• Diagnosis of Subacromial Impingement Syndrome (SIS) based on clinical criteria (pain with overhead activities, painful arc, positive Neer, Hawkins, or Jobe test). Radiological confirmation (ultrasound and/or magnetic resonance imaging) is accepted.
• Access to the internet and a device (smartphone, tablet, or computer) capable of running the telerehabilitation platform.
• Willingness and ability to provide written informed consent.

You may not qualify if…

• Shoulder pain caused by fractures, tumors, infections, or severe systemic pathologies.
• Previous surgery on the affected shoulder within the last 3 months.
• Prior joint injection (corticosteroid infiltration) in the affected shoulder within the last 3 months.
• Subjects with partial or full-thickness rotator cuff tears.
• Patients currently receiving concurrent physical therapy (PT) or any other external interventions for the shoulder condition.
• Current participation in another rehabilitation or exercise program.
• Pregnancy.
• Cognitive impairment, communication barriers, or any condition that prevents the patient from following the remote instructions.

Full record on ClinicalTrials.gov

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