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Interferential Current and Therapeutic Exercise Program in Chronic Neck Pain

U

University of Seville

Status

Completed

Conditions

Neck Pain

Treatments

Other: Interferential Current and Therapeutic Exercise Program
Other: Therapeutic Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT03979287
IFC Therapy and Exercise

Details and patient eligibility

About

Objectives: To analyze the number of sessions needed to achieve a positive impact after combining interferential current therapy and therapeutic exercise, compared with therapeutic exercise alone, on self-reported pain, disability and range of motion in subjects with chronic neck pain.

Design: A randomized, single-blind, controlled trial. Subjects: Patients between 18 and 65 years old, with idiopathic chronic neck pain.

Methods: The experimental group who will perform a combined treatment using Interferential current therapy and therapeutic exercise for two weeks. The control group will receive the same program of therapeutic exercise during the same period of time.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Nonspecific mechanical neck pain (chronic neck pain diagnosed by a physician)
  • Age between 18 and 65 years old
  • Both males and females
  • Non apprehension to electrotherapy (determined by the Personal Psychological Apprehension scale- EAPP)
  • Self-reported pain higher than 2 in the 11-point Numeric Pain Rating Scale

Exclusion criteria

  • Metallic implants in the vertebral column
  • Apprehension to electrotherapy (a score >45 points in EAPP)
  • Cervicogenic headache
  • Cervicogenic Dizziness
  • Neck pain associated with neurological deficits
  • Unexplained fever
  • Cervical surgery associated to persistent pain
  • Specific diagnostics (cervical myelopathy, cervical stenosis, osteomyopathy)
  • Other diagnostics such as visceral pain referred to the neck or non-cervical cause.
  • Involvement in litigation
  • Manual treatment for the neck-shoulder area in the last month before data collection

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

IFC and Therapeutic Exercise Program
Experimental group
Description:
Patients will receive 10 sessions for two weeks. The duration of each session will be of approximately one hour. Participants will receive treatment with Interferential current therapy plus a program of therapeutic exercise focused on the neck region
Treatment:
Other: Interferential Current and Therapeutic Exercise Program
Therapeutic Exercise Program
Active Comparator group
Description:
Patients will receive 10 sessions for two weeks. The duration of each session will be of approximately one hour.This group will only receive the same therapeutic exercise program.
Treatment:
Other: Therapeutic Exercise Program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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