Skip to content

Comparison of the Effectiveness of Stretching and Strengthening Exercises in Patients With Frozen Shoulder

Comparison of the Effectiveness of Stretching and Strengthening Exercises on Pain, Functional Status, Range of Motion and Psychosocial Factors in Patients With Frozen Shoulder

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06469502
Enrollment
56
Registered
2024-06-21
Start date
2024-07-01
Completion date
2025-08-15
Last updated
2024-06-21

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

Conditions

Frozen Shoulder

Keywords

frozen shoulder, exercise, stretching, strengthening

Brief summary

The aim of the study is to compare the effectiveness of stretching and strengthening exercises on pain, functional status, range of motion and psychosocial factors in patients with frozen shoulder.

Detailed description

Frozen shoulder is a common disorder characterized by spontaneous shoulder pain, progressive inflammation and fibrosis of the joint capsule and loss of both active and passive glenohumeral range of motion.Exercise reduces pain, increases range of motion and function in patients with frozen shoulder. When investigators examine the literature, stretching and strengthening exercises are frequently encountered in the content of multimodal exercise programs applied clinically and at home in frozen shoulder. However, they have not been compared in isolation. Stretching is known to increase flexibility, while strengthening is often used to increase strength capacity and hypertrophy.Both exercise methods produce mechanical tension, known as a factor that stimulates anabolic metabolism and increases protein synthesis.Therefore, the aim of the study is to compare the effectiveness of stretching and strengthening exercises on pain, functional status, range of motion and psychosocial factors in patients with frozen shoulder.According to the power analysis result, 56 patients will be randomized into two groups (Group 1 =28, Group 2=28). The treatment will last for a total of 6 weeks and the follow-up period will be 6 weeks. Group 1 will be included in the program consisting of stretching exercises only. Patients will receive a 6-week rehabilitation program consisting of 18 sessions of stretching exercises (3 times a week) under the supervision of a physiotherapist. Group 2 will be included in the program consisting of strengthening exercises only. Patients will receive a 6-week rehabilitation program consisting of 18 sessions of strengthening exercises (3 times per week) under the supervision of a physiotherapist. The primary outcomes are the Quick Disabilities of the Arm, Shoulder and Hand Questionnaire (Quick DASH) and the Numeric Pain Rating Scale (NPRS), while the secondary outcomes are the American Shoulder and Elbow Surgeons Standardized Shoulder Evaluation (ASES), Shoulder range of motion, Brief Pain Inventory-Short Form (BFI-SF) and Pain Catastrophizing Scale (PCS).

Interventions

PROCEDUREStretching Exercises

Group 1 will be included in the program consisting of stretching exercises only. Patients will receive a 6-week rehabilitation program consisting of 18 sessions of stretching exercises (3 times a week) under the supervision of a physiotherapist.

Group 2 will be included in the program consisting of strengthening exercises only. Patients will receive a 6-week rehabilitation program consisting of 18 sessions of strengthening exercises (3 times a week) under the supervision of a physiotherapist.

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Being between the ages of 40-65 * Clinical and radiologic diagnosis of unilateral primary frozen shoulder * Being in frozen shoulder stages 2 and 3 * Having an ROM of less than 50% in one or more directions of shoulder flexion, abduction, external rotation compared to the unaffected shoulder * Giving informed consent and volunteering * To have the ability to understand evaluation scales

Exclusion criteria

* Neurological, cardiovascular, cerebrovascular disease * Those with severe mental illness or impaired consciousness * Upper extremity fractures and tumors * Rheumatic disease * Pathologies of cervical origin * Untreated shoulder trauma * Severe osteoporosis * Previous treatment for the current complaint (physiotherapy and rehabilitation, intra-articular injection, surgery)

Design outcomes

Primary

MeasureTime frameDescription
Quick DASHbaseline, after 6 weeks and 6 weeks follow upQuick Disabilities of the Arm, Shoulder, and Hand: The Quick DASH is a 11-item questionnaire used to assess upper limb functionality. The score ranges from 0 (no disability) to 100 (most severe disability).
NPRSbaseline, after 6 weeks and 6 weeks follow upNumeric Pain Rating Scale: The pain was measured using a NPRS. Patients are asked to rate their pain ranging from 0 to 10 (0: no pain, 10: the worst pain imaginable)

Secondary

MeasureTime frameDescription
ASESbaseline, after 6 weeks and 6 weeks follow upThe American Shoulder and Elbow Surgeons Standardized Shoulder Assessment: The ASES score ranges from 0-100. Higher scores indicate better functional ability
Shoulder Range of Motion (ROM)baseline, after 6 weeks and 6 weeks follow upShoulder ROM measurements of forward flexion, abduction, and scapular plane external -internal rotation were taken using a standard goniometer. Pain-free active ROM and passive ROM were assesment.
BPI-SFbaseline, after 6 weeks and 6 weeks follow upBrief Pain Inventory-Short Form: The BPI is a two-factor instrument that measures pain severity and pain interference. The pain severity factor has four items, all rated on a 0-to-10 Likert scale: 0 corresponds to no pain and 10 corresponds to pain as bad as you can imagine. The pain interference factor has seven items, all rated on a 0-to-10 Likert scale: 0 corresponds to does not interfere and 10 corresponds to interferes completely.
PCSbaseline, after 6 weeks and 6 weeks follow upPain Catastrophizing Scale: Each item is scored from 0 (never) to 4 (always), giving a total score ranging from 0 to 52. Higher scores indicate higher levels of pain catastrophizing.

Countries

Turkey (Türkiye)

Contacts

Primary ContactÜmmü Öztürk, PhD(c)
ummuozturk90@hotmail.com05346749164
Backup ContactDerya Çelik, Professor
ptderya@hotmail.com05327940169

Outcome results

None listed

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