Effects of kinesiotaping on disability and pain in patients with rotator cuff tendinopathy

Effects of kinesiotaping on disability and pain in patients with rotator cuff tendinopathy: double blinded randomized clinical trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202007672254335

Enrollment

Registered

2020-07-21

Start date

2019-05-20

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Musculoskeletal Diseases

Interventions

kinesiotaping

placebo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: age between 20 and 60 years shoulder pain before 150° of active elevation in any plane positive signs of conflict (Neer's or Hawkins sign) on clinical examination.

Exclusion criteria

Exclusion criteria: progressive dermatological pathology contraindicating application of an adhesive shoulder bandage history of surgery, fracture or dislocation of shoulder intra-articular corticosteroid infiltration in the previous 6 months cervical or radicular signs hyperpilosis that may impede application of KT

Design outcomes

Primary

Measure	Time frame
Arabic version of the Disabilitiy of the Arm, Shoulder and Hand (DASH) questionnaire	—

Secondary

Measure	Time frame
Visual Analog Scale for pain at rest;Visual Analog Scale for pain at active movements;Visual Analog Scale for pain at night	—

Countries

Morocco

Contacts

Public ContactLatifa Tahiri

Mohammed V university of Rabat

latifatahiri@yahoo.fr+212661425506

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026