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Cervical Range of Motion and Stretching

University of Central Florida logo

University of Central Florida

Status

Completed

Conditions

Cervical Shortening

Treatments

Procedure: Manual stretching

Study type

Interventional

Funder types

Other

Identifiers

NCT03990324
BIO-17-13405

Details and patient eligibility

About

Cervical range of motion (ROM) is necessary to perform normal activities of daily living and deficits are associate with various pathologies. Currently, its unclear if specific myofascial stretches will improve cervical range of motion and decrease myofascial sensitivity. After a single session of the manual stretching procedure, participants immediately demonstrated increased cervical ROM and pressure pain thresholds.

Full description

Methods: Sixty participants with no history of neck pain or trauma were randomized into one of two groups: stretching group (n = 30), or control group (n = 30). The stretching group received a standardized manual stretching protocol. The control group did not received intervention. Pre and Post-test measurements were recorded for both groups. Within group differences and group by time interactions were evaluated for Cervical range of motion ROM and myofascial sensitivity. The immediate improvement in active ROM of the cervical spine may prompt clinicians to consider the sequencing of treatment. Stretching prior to active exercises may allow for active exercise through a larger ROM. Future research is needed to evaluate the immediate effects of stretching in the symptomatic population.

Enrollment

60 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ages of 18-60
  • active cervical flexion, right lateral flexion OR left cervical lateral flexion <45˚

Exclusion criteria

  • minors
  • prisoners
  • individuals with cognitive impairments
  • recent neck surgeries
  • pre-existing neck injuries

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Control group
No Intervention group
Description:
The control group did not received intervention and sat on a table for approximately 5 minutes
Stretching group
Experimental group
Description:
The stretching group received a standardized manual stretching protocol
Treatment:
Procedure: Manual stretching

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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