Health Condition 1: M248- Other specific joint derangements,not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participant provides written informed consent and agrees to voluntary participation in the study. Male and female participants aged 18 to 70 years. Medically diagnosed with Type 2 Diabetes Mellitus. Diagnosed with Frozen Shoulder also known as Adhesive Capsulitis based on the following: Shoulder pain of at least 3 centimeters on the Visual Analog Scale at rest or during activity for more than three months. Restriction in both active and passive shoulder range of motion. Normal shoulder radiographs. Individuals in Phase One or Phase Two of Frozen Shoulder. Vividness of Visual Imagery Questionnaire score between 16 and 48.
Exclusion criteria
Exclusion criteria: Patients presenting with shoulder dislocation, arthritis, fracture, avascular necrosis, or osteoporosis. History of surgery involving the neck or affected shoulder. Participants who have undergone any treatment such as corticosteroid injection in the shoulder or physiotherapy within the past one year. Douleur Neuropathique Four Questionnaire score of four or more. History of stroke or other neurological disorders affecting upper limb function. Participants with impaired sensation who may be unable to provide appropriate feedback regarding Transcutaneous Electrical Nerve Stimulation intensity. Participants with pacemaker or epilepsy, as these are contraindications for Transcutaneous Electrical Nerve Stimulation. Severe cardiac or respiratory illness that may interfere with physical activity. Diagnosed psychiatric illness or cognitive impairment that may interfere with study participation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.The Visual Analog Scale (VAS) 2.Short-Form 36-Item Health Survey (SF-36) 3. The Shoulder Pain and Disability Index (SPADI)Timepoint: Baseline,6 weeks, 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Tampa Scale of Kinesiophobia (TSK) The Pain Catastrophizing Scale (PCS) Universal GoniometerTimepoint: Baseline,6 weeks, 8 weeks | — |
Countries
India
Contacts
KLE College of Physiotherapy Hubballi.