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Evaluation of the Effectiveness of Night Orthosis in Treating Women With Symptomatic Osteoarthritis in the Interphalangeal Joint of the Dominant Hand

F

Federal University of São Paulo

Status

Completed

Conditions

Hand Injuries

Treatments

Device: Orthosis

Study type

Interventional

Funder types

Other

Identifiers

NCT02789852
PGSilva

Details and patient eligibility

About

Evaluation of the effectiveness of using a night orthosis for II and III or fingers of the dominant hand in women diagnosed with symptomatic osteoarthritis compared to a control group.

Full description

Objective: To evaluate the effectiveness of using a night orthosis for II and III or fingers of the dominant hand in women diagnosed with symptomatic osteoarthritis compared to a control group.

Methods: Through a randomized controlled clinical trial with blind assessment and follow-up of six months. Fifty-Two participants were randomized into two groups: group orthosis and control, and made a night orthosis II and or III fingers, thermoplastic will be used as a treatment for participants orthosis group. The participants underwent four evaluations at time 0, 45 days, 90 days and 180 days after its inclusion in the study. The variables studied were: the visual analog scale of pain, grip and pinch strength, questionnaires Cochin and Australian/Canadian Hand Osteoarthritis Index and functional Pick-up test.

Enrollment

52 patients

Sex

Female

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women aged between 40 and 80 years.
  • Patients diagnosed with osteoarthritis (OA) hand according to the American College of Rheumatology classification criteria.
  • Pain symptom in proximal interphalangeal (PIP's) or distal interphalangeal (DIP's) dominant hand in II and III or fingers.
  • Provide greater pain symptom of II and III or fingers between each other.
  • Complains of pain symptom measured by a visual analog scale (VAS) pain between 3 to 8 cm in the II and III or fingers of the dominant hand reported to perform joint movement (activity).
  • Thumb abduction with the II and III fingers without changing the pincer movement pulp-pulp.

Exclusion criteria

  • Other rheumatic diseases, neurological and skeletal muscle that can affect the upper limb.
  • Fibromyalgia uncontrolled.
  • Pregnancy.
  • Geographical inaccessibility and transport.
  • Cognitive impairment that prevents the understanding of assessment tools.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

52 participants in 2 patient groups

Orthosis Group
Experimental group
Description:
Will use the night orthosis for interphalangeal in the treatment of OA hand.
Treatment:
Device: Orthosis
Control Group
No Intervention group
Description:
wait for treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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