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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05771441
Other study ID # HYSHNP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date May 1, 2022

Study information

Verified date March 2023
Source Afyonkarahisar Health Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, we aimed to determine the effects of heat therapies and neck stabilization exercises on pain, disability, range of motion, and mood of NP patients.


Description:

Chronic non-specific neck pain (NP) has become one of the main causes of disability in the adult population around the world.Several treatment options used like; exercise, manual therapy, electrotherapy, and hot treatments etc. In this study, we aimed to determine the effects of heat therapies and neck stabilization exercises on pain, disability, range of motion, and mood of NP patients.100 patients with NP will be included.Patients will be randomyl assigned to 4 groups and will receive a total of 3 weeks of treatment. Patients' pain levels (visual analogoue scale VAS), quality of life (short form 36), mood (Beck deppression inventory BDI), range of motion, and neck disability index were evaluated prior to treatment, at 6th and at 12th weeks.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date May 1, 2022
Est. primary completion date May 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: Patients with chronic neck pain Exclusion Criteria: - sensory deficit on neck area, servical disc pathologies, neurological deficit, malignity, secondary causes for neck pain, active inflammation, arthritis on the neck area, serious mental health problems, pregnancy, spine surgery, and having received treatment to the cervical region in the last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
neck stabilization exercise (nse)
neck stabilization exercise (nse)- exercise
NSE + HOT PACK THERAPY
NSE + HOT PACK THERAPY- exercise plus heat therapy
NSE + infrared therapy
NSE + infrared therapy- exercise plus heat therapy
NSE + ultrasound therapy
NSE + ultrasound therapy exercise plus heat therapy

Locations

Country Name City State
Turkey Hilal Yesil Merkez Afyon

Sponsors (1)

Lead Sponsor Collaborator
Hilal Yesil

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary change from baseline VAS (visual analog scale) at 6th and 12th week The patients were asked to make an assesment of their pain level between 0 and 10 scale up to 12 weeks
Secondary Change from baseline quality of life (short form 36) at 6th and 12th week The physical and mental health summary scores were the primary components used. Scoring is on a scale of 0 to 100 and a higher score reflects better health-related quality of life. up to 12 weeks
Secondary Change from baseline shoulder range of motion (ROM) at 6th and 12th week The patients' joint range of motion will be measured with a goniometer. up to 12 weeks
Secondary Change from baseline Beck depression inventory (BDI) at 6th and 12th week A total Beck score (0-63) is obtained by giving each question a score of 0-3 in the survey. 17 is considered the threshold value for the degree of depression. up to 12 weeks
Secondary Change from baseline neck disability index (NDI) at 6th and 12th week Patient-completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation.
The NDI has sufficient support and usefulness to retain its current status as the most commonly used self-report measure for neck pain
up to 12 weeks
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