Home Exercises Protocol for Neck Pain

Sponsor
Universidade Federal de Pernambuco (Other)
Overall Status
Completed
CT.gov ID
NCT04187001
Collaborator
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. (Other)
27
1
22.6
1.2

Study Details

Study Description

Brief Summary

Delphi study about home exercise protocol development for neck pain.

Condition or Disease Intervention/Treatment Phase
  • Other: Content Validity
  • Other: Cultural adaptation

Detailed Description

Introduction: Neck pain is rising globally as a musculoskeletal disorder, as a result of several factors. Currently, there are several types of treatments for cervicalgia, applied according to the therapist's choice and patient's conditions and preferences, however, there are no reports of an effective self-performing treatment aiming to stabilizing the cervical, giving musculoskeletal balance, and focus on reducing pain.

It is important the promotion of a self-performing treatment, resulting in a high cost benefit because patient does not have to move to perform the treatment outside his or her home, does not need financial resources and demands little time to perform it. In addition to decreasing the frequency and intensity of hospitalizations and government costs incurred in this musculoskeletal disorder. Therefore, the study aims to construct, validate and adapt a self-performing exercise protocol in reducing cervical pain.

Methods: The first phase was the development of the first version of the protocol, through literature search; in the second phase, the content was validated, through evaluation by a committee of nine physiotherapists judges using the Delphi technique; and the last phase of the protocol, the cultural adequacy, is being performed through evaluation by fifteen participants of the target population to assemble the final version of the protocol.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
27 participants
Observational Model:
Other
Time Perspective:
Other
Official Title:
Home Exercises for Neck Pain: a Delphi Survey
Actual Study Start Date :
May 13, 2018
Actual Primary Completion Date :
Nov 11, 2019
Actual Study Completion Date :
Mar 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Judges

Professionals that assess the content validity of the exercise protocol

Other: Content Validity
Use Delphi technique for achieve consensus

Target population

People that assess the exercise protocol for cultural adaptation

Other: Cultural adaptation
Adapt the content to the target population

Outcome Measures

Primary Outcome Measures

  1. Concordance [february - may 2019]

    degree of consensus by percentage, content validity index

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Judges: physical therapists with at least 2 years of experience in cervical area.

  • Target population: chronic neck pain.

Exclusion Criteria:
  • Vestibular system problems, balance impairment, nervous system-related disorders, inability to perform exercises, history of cervical trauma or surgery in the region, history of cervical radiculopathy, history of cervical spine injury, temporomandibular dysfunction.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Federal University of Pernambuco Recife Pernambuco Brazil 50.740-560

Sponsors and Collaborators

  • Universidade Federal de Pernambuco
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

Investigators

  • Study Director: Gisela R Siqueira, PhD, Universidade Federal de Pernambuco

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Laylla Marjorye Rebouças Bezerra, Laylla Marjorye, Universidade Federal de Pernambuco
ClinicalTrials.gov Identifier:
NCT04187001
Other Study ID Numbers:
  • 3.007.662
First Posted:
Dec 5, 2019
Last Update Posted:
Apr 1, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Laylla Marjorye Rebouças Bezerra, Laylla Marjorye, Universidade Federal de Pernambuco
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 1, 2021