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Low Level Laser Therapy to Reduce Chronic Pain

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliImekamilika
Wadhamini
Erchonia Corporation

Maneno muhimu

Kikemikali

The purpose of this study was to determine whether low level laser light directed at the neck and shoulders could be effective in the temporary reduction of chronic pain in the neck and shoulder region.

Maelezo

Chronic neck and shoulder pain arising from osteoarthritis, chronic muscle spasms or thoracic or cervical spine sprain strain can be seriously debilitating. Currently available treatment options such as pain relief medication, ice pack, massage, physical therapy and chiropractic are typically of limited effectiveness. More permanent options such as surgery are invasive with long recovery periods and side-effects and complications of their own. Low level laser light therapy, with its proven anti-inflammatory ability, offers a simple non-invasive option for the reduction of chronic neck and shoulder pain.

Tarehe

Imethibitishwa Mwisho: 03/31/2014
Iliyowasilishwa Kwanza: 06/24/2009
Uandikishaji uliokadiriwa Uliwasilishwa: 06/25/2009
Iliyotumwa Kwanza: 06/28/2009
Sasisho la Mwisho Liliwasilishwa: 04/01/2014
Sasisho la Mwisho Lilichapishwa: 05/01/2014
Tarehe ya matokeo ya kwanza yaliyowasilishwa: 07/05/2009
Tarehe ya matokeo ya kwanza ya QC yaliyowasilishwa: 04/01/2014
Tarehe ya matokeo ya kwanza kuchapishwa: 05/01/2014
Tarehe halisi ya kuanza kwa masomo: 06/30/2000
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 08/31/2000
Tarehe ya Kukamilisha Utafiti: 08/31/2000

Hali au ugonjwa

Chronic Pain

Uingiliaji / matibabu

Device: Erchonia PL2000 Laser

Device: Placebo laser

Awamu

-

Vikundi vya Arm

MkonoUingiliaji / matibabu
Active Comparator: Erchonia PL2000 Laser
Low level laser light energy comprised of 1 milliWatts (mW) of red light (635 nm).
Device: Erchonia PL2000 Laser
Low level laser light therapy device that emits 1 mW of red (635 nm wavelength) light. It is a hand-held device that uses rechargeable batteries or a separate power adapter.
Placebo Comparator: Placebo laser
inactive light
Device: Placebo laser
Inactive laser light.

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Hupokea Wajitolea wa AfyaNdio
Vigezo

Inclusion Criteria:

- Muscular-skeletal pain in the neck/shoulder region

- Acute and chronic pain in the neck/shoulder region

- Restricted range of motion in the neck/shoulder region

- Fibrosis or scar tissue in the neck/shoulder region

- Inflammation in the neck/shoulder region

- Altered function in the neck/shoulder region

- Muscle strains in the neck/shoulder region

- Rating of 30 or greater on the 0-100 Visual Analog Scale (VAS) pain scale

- 18-65 years of age

Exclusion Criteria:

- Severely herniated disks

- Pregnancy

- Taken pain medication within the past 12 hours

Matokeo

Hatua za Matokeo ya Msingi

1. Number of Participants Whose Self-reported Degree of Pain on the Visual Analog Scale (VAS) in the Neck and Shoulder Area Decreased by 30% or More From Before to After Study Treatment. [baseline and one hour]

Self-reported degree of pain in the neck and shoulder region on the Visual Analog Scale (VAS). The VAS is a 100 mm long horizontal line ranging from '0: no pain at all' on one end to '100: worst pain imaginable' on the other end. Participants mark a point along the line that best represents the pain they are experiencing at that moment.

2. Change in Self-reported Degree of Pain in the Neck-shoulder Region on the 0-100 Visual Analog Scale (VAS) [baseline and one hour]

Self-reported degree of pain in the neck and shoulder region on the Visual Analog Scale (VAS). The VAS is a 100 mm long horizontal line ranging from '0: no pain at all' on one end to '100: worst pain imaginable' on the other end. Participants mark a point along the line that best represents the pain they are experiencing at that moment. The change is calculated as the difference from the VAS score recorded at baseline to the VAS score recorded one hour after study treatment administration. A positive change (+) means that the pain got worse and a negative change (-) means that the pain got better.

Hatua za Matokeo ya Sekondari

1. Change in Range of Motion (ROM) for the Left Side of the Neck From Baseline to One Hour After Study Treatment. [baseline and one hour]

Range of motion (ROM) for the left side of the neck is a measure of how well the neck can move to the left side. The participant gently tilts their neck to the left side as far as possible, and this distance is measured in degrees. The change for ROM for the left side of the neck is measured as the difference in degrees of ROM recorded from baseline to one hour after study treatment. If the change is positive (+), this means that ROM has gotten better and the neck can move further to the left side than before getting the treatment. If the change is negative (-), this means that ROM has gotten worse and the neck can move less to the left side than before getting the treatment

2. Change in Range of Motion (ROM) for the Left Shoulder From Baseline to One Hour After Study Treatment. [one hour]

Range of motion (ROM) for the left shoulder is a measure of how well the participant can move the left shoulder. The participant gently raises the left shoulder (and left arm) as far as possible, and this distance is measured in degrees. The change for ROM for the left shoulder is measured as the difference in degrees of ROM recorded from baseline to one hour after study treatment. If the change is positive (+), this means that ROM has gotten better and can move the left shoulder better and further than before getting the treatment. If the change is negative (-), this means that ROM has gotten worse and the left shoulder can move less easily and not as far than before getting the treatment

3. Change in Range of Motion (ROM) for the Right Side of the Neck From Baseline to One Hour After Study Treatment. [baseline and one hour]

Range of motion (ROM) for the right side of the neck is a measure of how well the neck can move to the right side. The participant gently tilts their neck to the right side as far as possible, and this distance is measured in degrees. The change for ROM for the right side of the neck is measured as the difference in degrees of ROM recorded from baseline to one hour after study treatment. If the change is positive (+), this means that ROM has gotten better and the neck can move further to the right side than before getting the treatment. If the change is negative (-), this means that ROM has gotten worse and the neck can move less to the right side than before getting the treatment.

4. Change in Range of Motion (ROM) for the Right Shoulder From Baseline to One Hour After Study Treatment. [baseline and one hour]

Range of motion (ROM) for the right shoulder is a measure of how well the participant can move the right shoulder. The participant gently raises the right shoulder (with right arm) as far as possible, and this distance is measured in degrees. The change for ROM for the right shoulder is measured as the difference in degrees of ROM recorded from baseline to one hour after study treatment. If the change is positive (+), this means that ROM has gotten better and the right shoulder can move further more easily than before getting the treatment. If the change is negative (-), this means that ROM has gotten worse and the right shoulder can move less and not as far to the left side than before getting the treatment.

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