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Efficacy of Eccentric Exercises in Individuals With Frozen Shoulder

Efficacy of Eccentric Exercises in Individuals With Frozen Shoulder: A Randomized Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04715035
Enrollment
40
Registered
2021-01-20
Start date
2022-08-03
Completion date
2025-06-27
Last updated
2025-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frozen Shoulder, Capsulitis, Adhesive, Capsulitis of Shoulder

Keywords

frozen shoulder, eccentric exercise, rehabilitation, physical therapy

Brief summary

Frozen shoulder is a musculoskeletal condition with a strong negative impact on activities of daily living, producing pain, disability, anxiety, and sleep disorders. It has a worldwide prevalence of 5.3%, increasing from 10 to 38% in patients with diabetes and thyroid conditions. This clinical entity manifests itself mainly in women between 40 and 65 years of age. Its resolution time is long and can reach 42 months with symptoms that persist throughout life. In the clinical evaluation, patients with Frozen Shoulder are manifested mainly by presenting mobility deficits. Previous studies described different structural alterations that may justify this clinical condition and its consequences, such as, for example, fibrosis of the coracohumeral ligament, alterations of the rotator interval, and of the axillary recess. Although passive structures are believed to be primarily involved in this condition, A series of five cases in which patients with frozen shoulder presented a significant increase in mobility after a general anesthetic block. The data obtained from this study and the different complications presented by patients with CH suggest that it is necessary to further understand the role of the rotator cuff in this clinical condition. Eccentric exercises consist of contracting the muscle to control or decelerate a load while the muscle or tendon is lengthening or remaining stretched. This intervention has been proposed for the treatment of tendinopathies in different body regions.

Detailed description

A randomized controlled clinical trial with two parallel groups will be carried out. Evaluators will be blinded to the treatment group and therapists will be unique to each group. This study will follow the CONSORT guidelines. Randomization by blocks between groups will be carried out through the website www.randomization.com and the sequence will be stored in sealed and opaque envelopes to maintain allocation confidentiality. This process will be carried out by an independent researcher, who will not be involved in the assessment and treatment. The allocation of subjects will be revealed to the researcher responsible for the treatment by opening the envelope before the start of the intervention. The researcher responsible for the evaluation will be blinded to the treatment group. The individuals will be blinded in relation to the study hypothesis and will not have contact with the participants of the same or the other group. Initially, all participants will undergo screening to assess the inclusion and non-inclusion criteria of the study. All individuals who meet the eligibility criteria will undergo an anamnesis to collect personal, sociodemographic, pain history, and primary and secondary outcomes measurements.

Interventions

mobilization, stretch, education, eccentric exercises

Sponsors

Hospital Durand, Argentina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* History of diffuse-onset shoulder pain of at least one month * Gradual loss of passive external rotation of at least 50% compared to the contralateral side

Exclusion criteria

\- History of shoulder fracture/ surgery * Shoulder pain reproduced by passive movement of the cervical spine * History of rheumatoid arthritis * Shoulder immobilization for more than 5 days * Bilateral frozen shoulder

Design outcomes

Primary

MeasureTime frameDescription
Shoulder FunctionFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.American Shoulder and Elbow Surgeons scale (ASES). This scale has a score between 0 to 100. When the score is more close to 0 Worst is the function of the shoulder and when is approximate 100, it is better.

Secondary

MeasureTime frameDescription
Perceived PainFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.The perceived pain is going to be assessed by a Visual Analogue Scale from 0 to 10, where the score close to 0 is worst, and approximate to 10 is better.
Pennation AngleFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.It is going to be assessed by an ultrasound device
Fear avoidanceFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.Fear Avoidance Beliefs Questionnaire This scale has a score between 0 to 96. When the score is more close to 96 worst is the fear avoidance and when is approximate to 0, it is better.
Range of MovementFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.An inclinometer will assess flexion, external rotation, and internal rotation range of movement. The higher the value, the better.
Muscle ThicknessFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.It is going to be assessed by an ultrasound device
Pain CatastrophizingFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.Pain Catastrophizing Scale (PCS)
Perceived Quality of lifeFrom enrollment to the end of treatment at 12 weeks. In the follow-up at 3 months and 9 months from the end of treatment.European Quality of Life Scale of five domains (EQ5D-3L). This scale has five items with a score between 1 to 3. When the score is more close to 3 worst is the quality of life and when is approximate to 1, it is better in each item. Also has a visual analogue scale of 100 points to assess the health condition, when the score is more close to 0 worst is the quality of life and when is approximate to 100 it is better.

Countries

Argentina

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026