Frozen ShoulderNCT07433478
Cervical and Thoracic Mobility Training in Patients With Adhesive Capsulitis
A study testing Convantional rehabilitation and Cervical and Thoracic Mobilization Exercises in people with Frozen Shoulder, run by Zonguldak Bulent Ecevit University at 1 site in Turkey (Türkiye).
Trial summary
The aim of this study is to investigate the effect of cervical and thoracic mobilization training on posture, shoulder pain, joint range of motion and shoulder function in patients with adhesive capsulitis. Read more about this study
- Who is it for?
- Ages 20 to 70 years
- Conditions the study is for
- Frozen Shoulder
- What is being tested?
- Convantional rehabilitation and Cervical and Thoracic Mobilization Exercises
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 6 Apr 2026to Aug 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Diagnosis of unilateral adhesive capsulitis
- Being between the ages of 20 and 70
Who cannot join
- Presence of glenohumeral joint osteoarthritis, dislocation, subluxation, fracture, tumor
- Rotator cuff injury
- Diagnosis of radiculopathy, rheumatological or neurological disease
- Presence of Thoracic Outlet Syndrome
- History of surgery on the affected upper extremity
- Any mental problem that would prevent compliance with tests and exercises
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of Cervical and Thoracic Mobility Training on Posture, Shoulder Pain, Range of Motion, and Shoulder Functionality in Patients With Adhesive Capsulitis
The aim of this study is to investigate the effect of cervical and thoracic mobilization training on posture, shoulder pain, joint range of motion and shoulder function in patients with adhesive capsulitis.
Read the detailed description
Adhesive capsulitis is a musculoskeletal disorder characterized by pain, stiffness, and a significant reduction in joint range of motion (ROM) in the shoulder joint, severely limiting daily living activities and functional capacity. The stiffness observed in the muscles and ligaments around the shoulder, especially after immobilization, leads to increased pain and restricted joint range of motion in the shoulder. All these pathological processes create a functional limitation cycle in the shoulder joint.
Postural imbalances and hypomobility occurring in the cervical and thoracic spine regions have a significant effect on the shoulder joint. The cervical and thoracic spine regions directly affect the biomechanics of the shoulder joint. Functional disorders in these regions cause decreased shoulder range of motion, irregular muscle activation, and increased pain. Postural disorders, particularly increased thoracic kyphosis and cervical protraction, negatively affect glenohumeral joint movements by altering the alignment of the shoulder girdle. These biomechanical abnormalities alter the normal position of the scapula, cause imbalance in muscle activation, and lead to functional impairment in the long term. When cervical alignment abnormalities are combined with thoracic hypomobility, the scapulothoracic rhythm is further disrupted, leading to increased shoulder pain.
Recent clinical studies have shown that thoracic mobility exercises are effective in treating adhesive capsulitis. Joint mobility exercises activate proprioceptive receptors, supporting pain modulation in the central nervous system and normalizing muscle activation patterns. Some studies have reported that adding thoracic mobility exercises to conventional physical therapy programs resulted in greater pain reduction, increased joint range of motion, and functional improvement compared to groups receiving physical therapy alone. These findings demonstrate that thoracic mobility exercises have both local and systemic effects.
According to relationship between the shoulder and thoracic spine, dysfunction in one anatomical region can lead to pain or restricted movement in a distant region. In this context, it is important to include not only the shoulder joint but also the thoracic and cervical spine in the treatment process for adhesive capsulitis. This ensures functional integrity, balances muscle activation, and accelerates the healing process.
Sensory inputs from the cervical spine play a role in head position and the synchronized functioning of the scapular muscles. In cases of cervical hypomobility, these proprioceptive inputs decrease, scapular stability is compromised, and postural control weakens. Therefore, cervical mobility exercises are important for supporting proprioceptive functions, correcting postural alignment, and restoring coordination of the scapular muscles. In conclusion, the current literature shows that cervical and thoracic mobility exercises are effective in reducing pain, increasing joint range of motion, correcting posture, and improving functional capacity in individuals with adhesive capsulitis.
However, the limited number of studies directly examining the effects of combined exercises targeting these two regions highlights the importance of randomized controlled trials in this area.
- Conditions
- Frozen Shoulder
- Being tested
- Convantional rehabilitation, Cervical and Thoracic Mobilization Exercises
- Keywords
- Frozen shoulder, Adhesizve capsulitis, mobilization
- Medical subject headings
- Bursitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Convantional rehabilitationOther
This group will have convantional rehabilitation exercises.
Cervical and Thoracic Mobilization ExercisesOther
This group will have convantional exercises, cervical mobilization and thoracic mobilization.
| Study group | Role | What they receive |
|---|---|---|
| Control Group | Active comparator | This group will undergo a program that includes posture exercises, wand exercises, Codman exercises, finger ladder exercises, and shoulder wheel exercises. Receives: Other: Convantional rehabilitation |
| Intervention Group | Experimental | This group will undergo a program that includes posture exercises, wand exercises, Codman exercises, finger ladder exercises, and shoulder wheel exercises and cervical and thoracic mobilization exercises in three sessions per week. Receives: Other: Cervical and Thoracic Mobilization Exercises |
What is being measured
The primary outcome is the main question the study is designed to answer.
Digital Goniometer Evaluation
Shoulder range of motion will be evaluated via digital goniometer. Flexion, extension, internal rotation and external rotation ranges will be recorded in degrees.
Measured: 3 weeks
Secondary outcomes (8)
Craniovertebral Angle Measurement
To assess head posture, craniovertebral angle measurement will be performed. A device with the relevant software installed will be used for the measurement. The angle will be measured for both the symptomatic and asymptomatic sides. Results will be recorded in degrees.
Measured: 3 weeks
Visual Analog Scale (VAS)
The Visual Analog Scale (VAS) will be used to evaluate pain for rest, activity and night periods. The data will be recorded in centimeters.On this scale, which is assessed by marking a line 10 centimetres long, the value "0" represents no pain, while the value "10" represents the most severe pain. As the score increases, the pain aggravates.
Measured: 3 weeks
Scapular Tilt
The distance between the acromion and the bed will be measured while the shoulders are relaxed and retracted on supine position. The results will be recorded in centimeters.
Measured: 3 weeks
Lateral Scapular Slide Test
This test is performed to determine the position of the scapula in the 0°, 45°, and 90° abduction positions of the shoulder. It is performed by determining the distance of the lower angle of the scapula from the corresponding thoracic spinal protuberance in the horizontal plane. All measurements will repeated 3 times and the results will be recorded in centimeters.
Measured: 3 weeks
Scapular Location Test
This test is performed to determine scapular elevation and rotation. Measurement points are marked by palpating the spinous process at the level of the medial end of the scapular spine, the medial end of the scapular spine, the lateral end of the scapular spine, the spinous process of the vertebra at the level of the lower end of the scapula, the lower end of the scapula, and the T12 spinous process. Using a tape measure, the distance between the spinous process of the vertebra at the same level as the medial end of the scapular spine and the spinous process at the level of the distal end of the scapula and the distance between the spinous process at the level of the distal end of the scapula and the spinous process of T12 will be measured and recorded in centimeters.
Measured: 3 weeks
Cervical and Thoracic Posture Assessment
The flexicurve tool will be used during the evaluation. Results will be recorded using millimeter measurement paper.
Measured: 3 weeks
Disabilities of the Arm, Shoulder and Hand Questionnare (DASH)
The DASH scale is a patient-reported questionnaire used to assess upper extremity function. The scale consists of 30 items scored from 1 to 5. When at least 27 items are completed, the responses to all items are summed to calculate the score. An algorithm is used to adjust for missing data, and the results are expressed as a standardized total score ranging from 0 to 100. This 30-item scale assesses upper extremity function, including pain and activities of daily living.
Measured: 3 weeks
Shoulder Pain and Disability Index (SPADI)
It was developed to assess the degree of shoulder pain and discomfort experienced by patients while performing daily living activities. The scale consists of a total of 13 items; 5 of these are pain-related, while 8 are disability-related. Each item is scored numerically from 0 to 10. The pain scale consists of 5 questions and is scored from 0 for "no pain" to 10 for "the most severe pain imaginable." The disability scale consists of 8 questions and is scored from 0 "no limitations" to 10 "unable to do." The total SPADI score is calculated by taking the percentage average of the pain and disability subscales. This score indicates the degree of the patient's shoulder pain and functional limitations in daily living activities.
Measured: 3 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Feb 2026
- Study start6 Apr 2026
- Primary completion3 Jul 2026
- Study completionAug 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Frozen ShoulderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Zonguldak Bulent Ecevit University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Eda AKBAŞ, Zonguldak Bulent Ecevit University
- Investigators
- Eda AKBAŞ, PhD, Study chair, Zonguldak Bulent Ecevit UniversityÖznur GÜNEY, MSc, Study chair, Zonguldak Bulent Ecevit UniversityMerve DEMİRCİ, MD, Principal investigator, Zonguldak Ataturk State Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07433478
- Sponsor's protocol ID
- BEUN-AKBAS-4
- Status last verified
- Feb 2026
- First submitted
- 20 Feb 2026
- Last updated
- 23 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 23 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Cervical and Thoracic Mobility Training on Posture, Shoulder Pain, Range of Motion, and Shoulder Functionality in Patients With Adhesive Capsulitis
- ClinicalTrials.gov ID
- NCT07433478
- Acronym / sponsor ID
- BEUN-AKBAS-4
- Conditions
- Frozen Shoulder
- Keywords
- Frozen shoulder, Adhesizve capsulitis, mobilization
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Zonguldak Bulent Ecevit UniversityUniversity, hospital or other
- Study start
- 6 Apr 2026 (actual)
- Primary completion
- 3 Jul 2026 (actual)
- Study completion
- Aug 2026 (estimated)
- First posted
- 25 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to investigate the effect of cervical and thoracic mobilization training on posture, shoulder pain, joint range of motion and shoulder function in patients with adhesive capsulitis.
Detailed description
Adhesive capsulitis is a musculoskeletal disorder characterized by pain, stiffness, and a significant reduction in joint range of motion (ROM) in the shoulder joint, severely limiting daily living activities and functional capacity. The stiffness observed in the muscles and ligaments around the shoulder, especially after immobilization, leads to increased pain and restricted joint range of motion in the shoulder. All these pathological processes create a functional limitation cycle in the shoulder joint.
Postural imbalances and hypomobility occurring in the cervical and thoracic spine regions have a significant effect on the shoulder joint. The cervical and thoracic spine regions directly affect the biomechanics of the shoulder joint. Functional disorders in these regions cause decreased shoulder range of motion, irregular muscle activation, and increased pain. Postural disorders, particularly increased thoracic kyphosis and cervical protraction, negatively affect glenohumeral joint movements by altering the alignment of the shoulder girdle. These biomechanical abnormalities alter the normal position of the scapula, cause imbalance in muscle activation, and lead to functional impairment in the long term. When cervical alignment abnormalities are combined with thoracic hypomobility, the scapulothoracic rhythm is further disrupted, leading to increased shoulder pain.
Recent clinical studies have shown that thoracic mobility exercises are effective in treating adhesive capsulitis. Joint mobility exercises activate proprioceptive receptors, supporting pain modulation in the central nervous system and normalizing muscle activation patterns. Some studies have reported that adding thoracic mobility exercises to conventional physical therapy programs resulted in greater pain reduction, increased joint range of motion, and functional improvement compared to groups receiving physical therapy alone. These findings demonstrate that thoracic mobility exercises have both local and systemic effects.
According to relationship between the shoulder and thoracic spine, dysfunction in one anatomical region can lead to pain or restricted movement in a distant region. In this context, it is important to include not only the shoulder joint but also the thoracic and cervical spine in the treatment process for adhesive capsulitis. This ensures functional integrity, balances muscle activation, and accelerates the healing process.
Sensory inputs from the cervical spine play a role in head position and the synchronized functioning of the scapular muscles. In cases of cervical hypomobility, these proprioceptive inputs decrease, scapular stability is compromised, and postural control weakens. Therefore, cervical mobility exercises are important for supporting proprioceptive functions, correcting postural alignment, and restoring coordination of the scapular muscles. In conclusion, the current literature shows that cervical and thoracic mobility exercises are effective in reducing pain, increasing joint range of motion, correcting posture, and improving functional capacity in individuals with adhesive capsulitis.
However, the limited number of studies directly examining the effects of combined exercises targeting these two regions highlights the importance of randomized controlled trials in this area.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control Group | Active comparator | Other: Convantional rehabilitationThis group will undergo a program that includes posture exercises, wand exercises, Codman exercises, finger ladder exercises, and shoulder wheel exercises. |
| Intervention Group | Experimental | Other: Cervical and Thoracic Mobilization ExercisesThis group will undergo a program that includes posture exercises, wand exercises, Codman exercises, finger ladder exercises, and shoulder wheel exercises and cervical and thoracic mobilization exercises in three sessions per week. |
Who may qualify
- Ages
- 20 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Diagnosis of unilateral adhesive capsulitis
- Being between the ages of 20 and 70
Key exclusion criteria (6 listed)
- Presence of glenohumeral joint osteoarthritis, dislocation, subluxation, fracture, tumor
- Rotator cuff injury
- Diagnosis of radiculopathy, rheumatological or neurological disease
- Presence of Thoracic Outlet Syndrome
- History of surgery on the affected upper extremity
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Convantional rehabilitationThis group will have convantional rehabilitation exercises. | Other | Control Group |
| Cervical and Thoracic Mobilization ExercisesThis group will have convantional exercises, cervical mobilization and thoracic mobilization. | Other | Intervention Group |
Primary outcome
Digital Goniometer Evaluation
Time frame: 3 weeks
Shoulder range of motion will be evaluated via digital goniometer. Flexion, extension, internal rotation and external rotation ranges will be recorded in degrees.
8 secondary outcomes
Craniovertebral Angle Measurement
Time frame: 3 weeks
Visual Analog Scale (VAS)
Time frame: 3 weeks
Scapular Tilt
Time frame: 3 weeks
Lateral Scapular Slide Test
Time frame: 3 weeks
Scapular Location Test
Time frame: 3 weeks
Cervical and Thoracic Posture Assessment
Time frame: 3 weeks
Disabilities of the Arm, Shoulder and Hand Questionnare (DASH)
Time frame: 3 weeks
Shoulder Pain and Disability Index (SPADI)
Time frame: 3 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Jul 2026.
- Individual participant dataSharing planned: Undecided
Related trials for Frozen Shoulder
Not yet recruiting
Effects of Posterior Capsular Stretching With and Without Dynamic Neuromuscular Stabilization Exercises in Frozen Shoulder
Frozen Shoulder
Active, not recruiting
Effects of Injection Combined With Spencer Technique on Painful Frozen Shoulder
Frozen Shoulder
RecruitingPhase 4
Ultrasound-Guided Intra-Articular vs Gluteal Intramuscular Corticosteroid Injection for Frozen Shoulder
Frozen Shoulder
Not yet recruitingPhase 4
OMT for Adhesive Capsulitis
Adhesive Capsulitis of the Shoulder, Frozen Shoulder
Recruiting
Maitland Mobilization With and Without Stroking Release Technique of Rotator Cuff Muscle in Frozen Shoulder
Adhesive Capsulitis
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Eda AKBAŞ, PhD study chair
Zonguldak Bulent Ecevit University
Öznur GÜNEY, MSc study chair
Zonguldak Bulent Ecevit University
Merve DEMİRCİ, MD principal investigator
Zonguldak Ataturk State Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Convantional rehabilitation and Cervical and Thoracic Mobilization Exercises in people with Frozen Shoulder, run by Zonguldak Bulent Ecevit University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 23 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Digital Goniometer Evaluation (time frame: 3 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jul 2026.