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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).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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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.

Turkey (Türkiye)1 site
  • Zonguldak Ataturk State Hospital

    Zonguldak

Other trials in Turkey (Türkiye)

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 groups in NCT07433478
Study groupRoleWhat they receive
Control GroupActive comparatorThis 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 GroupExperimentalThis 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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.

  1. First posted25 Feb 2026
  2. Study start6 Apr 2026
  3. Primary completion3 Jul 2026
  4. Study completionAug 2026 (estimated)

Resources

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)
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

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.

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