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CompletedNCT05395572Updated May 27, 2022

The Effects of Kinesio® Tape on Neck Pain and Disability

An interventional study of Kinesio® Tape in Neck Pain, sponsored by North Dakota State University. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2022-05-27.

Sponsored by North Dakota State University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Non-randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This study is a within-subjects design; therefore, the participant will serve as their own control. Participants will be included in the study if they have neck pain or disability defined by a score of more than 14 on the Neck Disability Index. They will be excluded if they have any diagnosed disc pathology. A mask-associated pain questionnaire will be completed by the participants prior to the study to determine their perceived effect of mask-wearing on neck pain. This questionnaire is adapted from the HAPPE study on mask-associated headache pain. A baseline pain rating will be recorded a numerical pain scale. Next, active cervical range of motion will be measured, three times in each direction to be averaged. A pain rating will be recorded for pain during cervical motion. Kinesio® Tape will be applied to activate the cervical extensor muscles. The participant will sit with the tape on for 20 minutes, then active cervical range of motion and pain will be recored again.

02

Conditions studied

  • Neck Pain

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03

In context

Neck Pain

1,233 studies on the registry are indexed under Neck Pain; 256 are open to participants now.

This study's enrollment of 30 is below the median of 51 across 1,005 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

North Dakota State University is the lead sponsor of 21 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
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Neck Disability Index Score of more than 14

Exclusion criteria

Exclusion Criteria:

  • cervical disc pathology or injury
  • previous neck surgery
  • prior history of general medical conditions involving joints, muscles, bones or connective tissue such as fibromyalgia, osteoporosis, etc.
  • an NDI score of less than 14 or more than 24
  • reported allergies to Kinesio® Tex Tape or any other adhesive material
  • any contraindications for the usage of Kinesio® Tape
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Tape

    Kinesio tape will be applied to the neck to help facilitate underactive muscles and ROM will be assessed

    Device: Kinesio® Tape

  • No intervention
    Control

    ROM will be assessed before tape application to determine any changes

Interventions

  • DeviceKinesio® Tape

    In order to increase the activity of underactive muscles, the tape is applied from origin to insertion with a 15-25% tension. The Kinesio® Tape mechanical muscle correction will be performed with one Y-strip of Kinesio® Tape over the bilateral cervical multifidus and semispinalis cervicis muscles, while also including portions of other cervical extensor muscles (the semispinalis capitis, splenius cervicis, levator scapulae, upper trapezius, longus coli, and splenius capitis).

06

What researchers measure

Primary outcomes

  1. Neck Disability Index

    Patient-reported neck pain

    Time frame: 1 day

  2. Headaches Associated With Personal Protective Equipment

    Mask associated pain questionnaire

    Time frame: 1 day

  3. Dartfish

    2-dimensional motion analysis

    Time frame: 20 minutes

07

Study locations

1 site
  • North Dakota State University
    Fargo, North Dakota 58108, United States
08

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 May 27, 2022, 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
NCT05395572
Lead sponsor
North Dakota State University
Responsible party
Sponsor
First posted
May 27, 2022
Start date
Mar 17, 2021
Primary completion
May 17, 2021
Completion
May 17, 2021
Last update
May 27, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2021. You cannot join it, but the record below documents what was studied.

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