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CompletedNCT02850549Updated Aug 1, 2016

Preliminary Neck Classification Study

An interventional study of Procedure: physical therapy and Neck Pain Classification in Neck Pain, sponsored by St. Ambrose University. Completed at 7 sites in United States. Per ClinicalTrials.gov, last updated 2016-08-01.

Sponsored by St. Ambrose University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
17
Allocation
Not applicable
Sex
All
01

Study summary

The purpose of this study was to assess if pain and function in patients with neck pain is less when physical therapists use a classification system.

Read the detailed description

The purpose of this study was to prospectively assess pain and function scores in patients with neck pain, with therapists specifically trained to implement a treatment based classification and matched interventions system. This study consisted of two phases to determine whether implementing a classification changed patient outcomes. In phase one, baseline data was obtained while physical therapists continued with their current neck pain evaluation and intervention approaches. The second phase involved educating the therapists in the neck classification system with the matched interventions. Pain and function outcomes were analyzed for 2 phases. The overall goal was to prospectively determine if the implementation of this classification system with matched interventions could enhance patient outcomes.

02

Conditions studied

  • Neck Pain

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Keywords

  • neck pain
  • cervical
  • classification
  • outcomes
  • physical therapy
03

In context

Neck Pain

1,259 studies on the registry are indexed under Neck Pain; 256 are open to participants now.

This study's enrollment of 17 is below the median of 52 across 1,026 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

St. Ambrose University is the lead sponsor of 7 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Licensed physical therapists
  • Treat patients with neck pain on a regular basis

Exclusion criteria

Exclusion Criteria:

  • Do not utilize interventions included in the study
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
17 participants (actual)

Study arms

  • Other
    physical therapy

    Physical Therapy intervention provided by therapists in phase one without training in following a neck classification system and in phase two after being trained to follow a neck pain classification system.

    Other: Procedure: physical therapy and Neck Pain Classification

Interventions

  • OtherProcedure: physical therapy and Neck Pain Classification

    Physical therapists treated patients in phase one as they usually do and in phase two were trained to follow a neck classification and matched intervention system.

06

What researchers measure

Primary outcomes

  1. Numeric Pain Rating (NPR)

    NPR was measured on initial evaluation and at the time the patient was discharged from care which varied for each patient (ranged from 3 to 107 days).

    Time frame: up to 107 days

  2. Neck Disability Index (NDI)

    NDI was measured on initial evaluation and at the time the patient was discharged from care which varied for each patient (ranged from 3 to 107 days).

    Time frame: up to 107 days

Secondary outcomes

  1. Number of Visits

    Time frame: Measured from initial evaluation to time of discharge from care; up to 107 days.

  2. Duration of Care

    Time frame: Number of days of care, measured from initial evaluation to time of discharge from care; up to 107 days.

07

Study locations

7 sites
  • Genesis Physical Therapy - King Plaza
    Moline, Illinois 61265, United States
  • Genesis Physical Therapy - Illini
    Silvis, Illinois 61282, United States
  • Genesis Physical Therapy - Maplecrest
    Bettendorf, Iowa 52722, United States
  • Genesis Physical Therapy - Lombard
    Davenport, Iowa 52803, United States
  • Genesis Physical Therapy - 53rd St
    Davenport, Iowa 52807, United States
  • Genesis Physical Therapy - Valley Fair
    Davenport, Iowa 52807, United States
  • Genesis Physical Therapy - Le Claire
    Le Claire, Iowa 52748, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02850549
Lead sponsor
St. Ambrose University
Responsible party
Kevin Farrell (Principal Investigator, St. Ambrose University) — Principal investigator
First posted
Aug 1, 2016
Start date
Oct 2011
Primary completion
Jan 2014
Completion
Jan 2014
Last update
Aug 1, 2016

Study contacts

Kevin Farrell
principal investigator · St. Ambrose University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2016. You cannot join it, but the record below documents what was studied.

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