NCT01465932

Brief Summary

The program of stretching, strengthening and proprioception is more effective than stretching and strengthening program in nursing, with rotator cuff disorder, according to indicators of quality of life and job satisfaction.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2010

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2010

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2011

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2011

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

October 25, 2011

Completed
13 days until next milestone

First Posted

Study publicly available on registry

November 7, 2011

Completed
Last Updated

November 7, 2011

Status Verified

October 1, 2011

Enrollment Period

11 months

First QC Date

October 25, 2011

Last Update Submit

November 4, 2011

Conditions

Keywords

Nursing staffPhysical Therapy (Specialty)

Outcome Measures

Primary Outcomes (1)

  • Indicators of quality of life (WORC - Western Ontario Rotator Cuff The Index)

    The WORC was selected to be a reliable tool for measuring quality of life for patients with rotator cuff disorder,available in Portuguese and validated for Brazilian culture by Lopes et al (2008). The WORC consists of 21 items and has five fields, and you can get the total for each domain separately. The domains are: physical symptoms, sports and recreation, work, lifestyle and emotions. The total score ranges from zero to 2100. Thus, zero implies no reduction in quality of life and the worst score is 2100.

    This scale is applied one day before and one day after the application of physical therapy intervention programs

Secondary Outcomes (1)

  • Questionnaire used was the Job Satisfaction Scale - Occupational Stress Indicator (OSI).

    This scale is applied one day before and one day after the application of physical therapy intervention programs

Study Arms (2)

No proprioception

ACTIVE COMPARATOR

Nursing professionals to diagnose disorders of the rotator cuff previously randomly allocated in this group did stretching exercises of the muscles of the cervical spine and chest, strengthening the muscles of the rotator cuff and stabilizers of the scapula, in addition to cryotherapy reduction of pain.

Other: Control, no Proprioception

Proprioceptive exercises

EXPERIMENTAL

Nursing professionals to diagnose disorders of the rotator cuff previously randomly allocated in this group did stretching exercises of the muscles of the cervical spine and chest, strengthening the muscles of the rotator cuff and stabilizers of the scapula, proprioception exercises to improve motor control, besides cryotherapy for reduction of pain.

Other: Experimental, Proprioceptive exercises

Interventions

The period of data collection period was from June 2010 to August 2011. All subjects who met the inclusion criteria, were randomly allocated to group 1 (control) or group 2 (experimental). Both groups consisted of 12 physical therapy sessions, taking place 2 times a week for 6 weeks. After randomization, subjects were allocated to group 1 (control group) underwent cervical stretching exercises, strengthening the scapular muscles and rotator cuff and cryotherapy.

Also known as: No proprioception
No proprioception

The period of data collection period was from June 2010 to August 2011. All subjects who met the inclusion criteria, were randomly allocated to group 1 (control) or group 2 (experimental). Both groups consisted of 12 physical therapy sessions, taking place 2 times a week for 6 weeks. After randomization, subjects were allocated to group 2 (experimental group) underwent cervical stretching exercises, strengthening the scapular muscles and rotator cuff exercises and cryotherapy as well as proprioceptive sensory-motor

Also known as: Proprioceptive exercises
Proprioceptive exercises

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • working as a nurse
  • technician or nursing assistant in the hospital
  • make medical diagnosis of disorder in the rotator cuff (impingement, injury or rupture of the cuff)
  • does not make a medical diagnosis of cognitive impairment
  • were receiving no another type of treatment for shoulder pain (eg medicines,acupuncture, massage)
  • availability and interest in participating in therapy and accept to participate in the survey.

You may not qualify if:

  • patients with pain that would prohibit their participation in the program with a medical diagnosis of cognitive impairment,
  • associated with debilitating diseases,
  • previous surgery of the shoulder,
  • other specific conditions of the shoulder joint (adhesive capsulitis,
  • degenerative osteoarthritis of the glenohumeral joint,
  • tendon calcification) and do not accept to join the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hospital of Clinics, University of Medicine of Ribeirao Preto

Ribeirão Preto, São Paulo, 055, Brazil

Location

Related Publications (1)

  • Martins LV, Marziale MH. Assessment of proprioceptive exercises in the treatment of rotator cuff disorders in nursing professionals: a randomized controlled clinical trial. Rev Bras Fisioter. 2012 Nov-Dec;16(6):502-9. doi: 10.1590/s1413-35552012005000057. Epub 2012 Nov 2.

MeSH Terms

Conditions

Shoulder Impingement SyndromePersonal Satisfaction

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and InjuriesBehavior

Study Officials

  • Lisandra V. Martins, postgraduate

    University of Sao Paulo

    PRINCIPAL INVESTIGATOR
  • Maria HP Marziale

    University of Sao Paulo

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lisandra Vanessa Martins

Study Record Dates

First Submitted

October 25, 2011

First Posted

November 7, 2011

Study Start

July 1, 2010

Primary Completion

June 1, 2011

Study Completion

August 1, 2011

Last Updated

November 7, 2011

Record last verified: 2011-10

Locations