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Dry Needling and Therapeutic Exercise on Sleep in Individuals With Chronic Neck Pain and Sleep Disturbance

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Mayo Clinic

Status

Active, not recruiting

Conditions

Sleep Disturbance
Neck Pain

Treatments

Other: Therapeutic Exercise
Procedure: Dry Needling

Study type

Interventional

Funder types

Other

Identifiers

NCT06275074
23-007716

Details and patient eligibility

About

Feasibility study investigating the effects of dry needling on individuals with chronic neck pain and sleep disturbance.

Full description

The purpose of this pilot study is to determine the feasibility of a large randomized clinical trial (RCT) which aims to investigate the effects of dry needling (DN) in addition to therapeutic exercise (TE) on sleep duration and quality in patients with chronic neck pain (CNP) and sleep disturbance (SD). Specifically, the objective is to explore feasibility of a study protocol and examine the preliminary data of a small sample size for the effectiveness of DN and TE for individuals with CNP and SD to determine effect size of the intervention.

Enrollment

28 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Neck pain lasting greater than 3 months 28,29
  • Age: 18-75 years
  • Presence of sleep disturbance - to be defined as a score ≥ 8 on the Insomnia Severity Index
  • Ability to understand study procedures and to comply with them for the entire length of the study

Exclusion criteria

  • Previous surgery to the neck or thoracic spine

  • Central nervous system disorders

  • Systemic joint disease (e.g. rheumatoid arthritis)

  • Infection

  • Cancer

  • Raynaud's disease

  • Pregnancy

  • Immunocompromised disease (e.g., diabetes mellitus, HIV, AIDS, lupus)

  • Insufficient English-language skills to complete all questionnaires.

  • Contraindications to dry needling:

    • Presence of needle phobia
    • History of abnormal reaction to needling or injection
    • History of bleeding disorder (e.g., current anticoagulant therapy or known thrombocytopenia)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

28 participants in 2 patient groups

Dry Needling and Therapeutic Exercise
Experimental group
Treatment:
Procedure: Dry Needling
Other: Therapeutic Exercise
Therapeutic Exercise Alone
Active Comparator group
Treatment:
Other: Therapeutic Exercise

Trial contacts and locations

1

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Central trial contact

Ray Lunasin, P.T., D.P.T.

Data sourced from clinicaltrials.gov

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