Effect Of Therapeutic Ultrasound When Given On Shoulder Capsule With a Sustained Stretch And End Range Mobilization On Pain,Range Of Motion And Disability In Individuals With Adhesive Capsulitis

Effect Of Therapeutic Ultrasound On A Sustained Capsular Stretch And End Range Mobilization On Pain, Range Of Motion And Disability In Individuals With Adhesive Capsulitis: A Randomised Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/10/095978

Enrollment

Registered

2025-10-13

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Therapeutic Ultrasound on sustained capsular stretch: Therapeutic Ultrasound on sustained capsular stretch and end range mobilization done for 10 sessions over a period of 2 weeks Contr

Eligibility

Inclusion criteria

Inclusion criteria: All genders aged between 40 to 65 years with stage 2 or 3 adhesive capsulitis Pain ranging between 3 to 7 on VAS Restricted range of motion for more than 3 months Both diabetic and non diabetic individuals If diabetic HbA1c levels should be equal to or more than 6.5 percentage Willingness to participant in the study

Exclusion criteria

Exclusion criteria: Diagnosed case of rotator cuff tears or other injuries to shoulder or elbow Diagnosed case of rheumatological disorders Malignancy adhesive capsulitis secondary to fractures dislocation reflex sympathetic dystrophy neurological disorder Recent fractures or shoulder surgeries on the same shoulder in the past 6 months History of arthritis related to shoulder Systemic inflammatory conditions or contraindications to ultrasound therapy

Design outcomes

Primary

Measure	Time frame
Visual analog scale VAS for Pain Universal goniometer for Range Of Motion Timepoint: outcome measures assessed at baseline and post intervention of 2 weeks	—

Secondary

Measure	Time frame
Disability of arm shoulder & hand DASH for disability & functionTimepoint: Outcome measure will be assessed at baseline & post intervention at 2 weeks	—

Countries

India

Contacts

Public ContactKunal V Tegginmani

KAHER Institute of Physiotherapy Belagavi

anandheggannavar@klekipt.edu.in9945282896

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026