Skip to content

Comparison Between Soft Tissue Mobilization and Strengthening Exercises in Management of Local Neck Syndrome

Comparison Between Soft Tissue Mobilization and Strengthening Exercises in Management of Local Neck Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05227963
Enrollment
30
Registered
2022-02-08
Start date
2016-04-04
Completion date
2021-08-20
Last updated
2022-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain, Neck Pain

Keywords

Assessment, Neck pain, Pain measurements, Patient outcome assessment, Treatment outcome

Brief summary

A single-blinded, parallel-group randomized controlled trial was conducted at the national institute of rehabilitation medicine, Pakistan, from April to July 2016, on 30 females who were recruited through non-probability convenient sampling technique and randomly allocated to the experimental and control group.

Detailed description

The experimental group received STM and neck isometric strengthening exercises, whereas the control group received neck isometrics strengthening exercises only. Numeric Pain Rating Scale (NPRS) was used to assess the pain intensity, while Neck Disability Index (NDI) was used to assess the neck-related disability. The data was collected pre-, during, and post-intervention. Repeated measure analysis of variance (RM ANOVA) was used to analyze within the group changes, while independent t-test was used to analyze the differences between the groups. Data were analyzed by using SPSS version 21. This study describes the comparative effectiveness of STM when used as adjunct to strengthening exercises and when strengthening exercises are used alone for the management of TNS. According to the results of this study, STM in combination with neck isometric strengthening exercises as well as exercises alone were effective for managing neck pain and functional disability when a comparison was made within the groups.

Interventions

In this group, each participants received 45-minutes long session that includes 25-minutes of soft tissue mobilization and 20-minutes of neck isometric strengthening exercises. In each session, patient was seated on chair and sustained pressure, direct oscillation, perpendicular mobilization, parallel mobilization, and friction massage was applied on the neck musculature for a minute followed by a release for 30 seconds. This protocol was repeated three times in each session. Each session was repeated four-times a week for two-weeks (a total eight sessions).

OTHERneck isometric strengthening exercises

In this group, each participant received 20-minutes long session. Each session started in seated position and participants were asked to perform flexion, extension, side bending and rotation against resistance. During flexion movement, therapist placed hand on forehead and asked patient to move the neck forward, while in extension, therapist hand was placed at back of the head and patient had to move neck in backward direction. However, in side bending and rotation- therapist hand was placed at lateral side of the head and asked patient to side bend the neck and look at shoulder in the same direction respectively. Each session was repeated four-times a week for two-weeks (a total eight sessions).

Sponsors

Health Education Research Foundation (HERF)
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Masking description

Non-probability convenient sampling technique was used to recruit the sample through lottery method into two groups.

Intervention model description

The randomized control study was conducted in two groups,one was experimental group received soft tissue mobilization and other was control group received strengthening exercises with supportive treatment for both groups.

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

:• Age above 30 and below 75 years * Patients having local neck pain included * Female included * With chronic neck syndrome (\> month)

Exclusion criteria

* Age below 30 and more than 75 years * Patients having radiating pain excluded * Male excluded. * With acute neck syndrome (\< 3 month)

Design outcomes

Primary

MeasureTime frameDescription
Numerical pain rating scale (NPRS)upto 2 weeksNPRS was used to assess the pain intensity. The 11-point numeric scale ranging from 0-10; 0 means no pain while 10 means worst possible pain.
Neck disability index (NDI)upto 2 weeks.NDI was used to assess the neck-related disability. Of the 50 score, 0-4 means no disability while 35-50 means severe disability.
Neck range of motionupto 2 weeks .Goniometer was used to measure the range of motion of neck.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026