NCT01381380

Brief Summary

This study is a pain intensity evaluation in patients with myofascial pain submitted kinesitherapy after trigger point injection.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2006

Typical duration for not_applicable

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2006

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2007

Completed
2.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2009

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

June 23, 2011

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 27, 2011

Completed
Last Updated

June 27, 2011

Status Verified

November 1, 2007

Enrollment Period

1 year

First QC Date

June 23, 2011

Last Update Submit

June 24, 2011

Conditions

Myofascial Pain Syndromes

Keywords

myofascial paintrigger point injectionmanual therapy

Outcome Measures

Primary Outcomes (1)

  • Pain intensity

    once a week for 8 weeks (T1 to T8)

    8 weeks

Study Arms (1)

single-arm studies

OTHER

Manual therapy for one group

Procedure: Manual therapy

Interventions

Manual therapyPROCEDURE

Manual therapy, once a week for 8 weeks

Also known as: massage, finger pressure, myofascial release, mobilization
single-arm studies

Eligibility Criteria

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

You may qualify if:

  • myofascial pain of neck and shoulder girdle, lasting ≥ 4 months, pain intensity ≥ 4.

You may not qualify if:

  • arrhythmia
  • heart block
  • coagulopathy
  • cognitive alterations and infection at the site
  • patients using anticoagulants, and pregnant women

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Setor de Dor

São Paulo, São Paulo, 04023-062, Brazil

Location

MeSH Terms

Conditions

Myofascial Pain Syndromes

Interventions

Musculoskeletal ManipulationsMassageMyofascial Release Therapy

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal Diseases

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitationTherapy, Soft Tissue

Study Officials

  • Rioko K Sakata, PhD

    Universidade Federal de São Paulo

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

June 23, 2011

First Posted

June 27, 2011

Study Start

November 1, 2006

Primary Completion

November 1, 2007

Study Completion

December 1, 2009

Last Updated

June 27, 2011

Record last verified: 2007-11

Locations

BR(1)