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CompletedNCT05624021Updated Nov 23, 2022

Effect of Functional Training and Isometric Exercises on Pain, ROM, and Functional Status in Patients With Neck Pain

An interventional study of Scapular functional training and Cervical isometric exercises in Chronic Pain, sponsored by King Saud University. Completed at 1 site in Saudi Arabia. Open to participants aged 22 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-11-23.

Sponsored by King Saud University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 2 months after the study started (first participant enrolled Aug 2019, registered Nov 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
22 Years to 35 Years
Sex
All
01

Study summary

Work-related musculoskeletal disorders have been rising fast around the globe leading to neck pain and scapular muscle dysfunction, contributing to a decrease in neck movements and functional limitations. This study aimed to determine the efficacy of scapular functional exercise (SFE) in combination with cervical isometric exercises (CIE) on neck pain, cervical range of motion, and functional limitations among participants with chronic mechanical neck pain.The study was based on a two-arm parallel group pretest-posttest randomized control trial design. Thirty participants (females 21 and males 9; average age 28.94±3.77 years) were randomly allocated to groups A and B (n=15/group). The group's A and B participants received a common intervention, such as CIE and hot packs. However, group A received the SFE in addition to common interventions. The outcomes, such as neck pain, cervical ROM, and functional limitations, were evaluated using a numeric pain rating scale (NPRS), standard universal goniometer, and neck disability index questionnaire at baseline and 4-week post-intervention. The paired and unpaired t-test was used to analyze the intervention effects on the outcomes within-group and between-group, keeping the significance level alpha set at p\<0.05.

Read the detailed description

The study hypothesised that adding the scapular functional training to the cervical isometric exercises will be equally effective than cervical isometric exercises alone on managing neck pain, cervical ROM, and functional limitations among participants with chronic mechanical neck pain. The present study is helpful for chronic mechanical neck pain patients and physiotherapist to better understand the effect of incorporation of the scapular functional training in the treatment of neck pain. Therefore, this protocol may be used as a treatment in chronic mechanical neck pain because it alleviates pain, neck disability, improving cervical range of motion in chronic mechanical neck pain.

02

Conditions studied

  • Chronic Pain

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Keywords

  • Chronic pain
  • Range of motion
  • Functional limitations
  • Isometric exercises
  • Functional training
03

In context

Chronic Pain

2,998 studies on the registry are indexed under Chronic Pain; 706 are open to participants now.

This study's enrollment of 30 is below the median of 60 across 2,209 interventional studies indexed under Chronic Pain.

Browse Chronic Pain studies →

Lead sponsor

King Saud University is the lead sponsor of 168 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
22 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Both male and female with aged range 22-35 years
  • Neck pain of more than 3 months in duration
  • Having neck pain without symptoms distal to shoulder
  • Participant had not received any clinical treatment for their neck pain within 1-months, and
  • Willingness to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Having a diagnosis of cervical spinal stenosis
  • Patients with serious pathology (e.g., neoplasm, fractures and inflammatory diseases, unilateral and bilateral upper extremity radicular symptoms (cervical radiculopathy)
  • Prior surgery of cervical spine
  • Evidence of nerve root compression
  • Pregnant women, and
  • Showed poor cooperation in the study
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    SFT group

    Received Scapular functional training and cervical isometric exercises

    Other: Scapular functional training · Other: Cervical isometric exercises · Other: Moist heating

  • Active comparator
    Conventional group

    Received only isometric cervical exercises and heating

    Other: Cervical isometric exercises · Other: Moist heating

Interventions

  • OtherScapular functional training

    The scapular functional training consists of press up and push up plus. Press up was done in sitting position on the training bench, feet on the floor with straight arm and the palms on the edge of the bench fingers pointing forward and then lift off and dip down just in front of the seat by moving the shoulder girdle. Progression is done by placing weight on the thigh. Push-up plus exercise started from a push up position on the hand, feet or knees and keeping the torso rigid by bracing the abdominals followed by protracting the scapula as high as possible. Progression is done moving from knees to the feet or adding resistance on the upper back. The training continued for three sessions per week for four weeks.

  • OtherCervical isometric exercises

    The isometric neck exercises taught to all the participants to perform in neutral sitting positions at home thrice a day for 15-days continuously. The sequences of exercises were shoulder circling in clockwise and anticlockwise direction, scapular retraction with cervical retraction, neck flexion, extension, either side of lateral bending/flexion, left and right rotation. Each exercise follows a set of 10 repetition of maximum voluntary contraction with a progressive hold time of 3, 5, 7, and 10 seconds depending on the severity of pain and tolerance of the participants.

  • OtherMoist heating

    A hydrocollator moist heat packs was applied over back of the neck in supine position to receive optimal heating. It was given for 20 minutes/day, five-day a week for four-week.

06

What researchers measure

Primary outcomes

  1. Neumeric pain rating scale (NPRS)

    Neck pain was assessed by a nuemeric pain rating scale. It is an 11-points numeric scale marked with 0 to 10 between either end. Zero at one end and ten at the opposite end indicate no pain and unbearable/worst imaginable pain, respectively. The participants were asked to rate their current level of pain, as well as their worst and least amounts of pain in the past 24 hours.

    Time frame: 4 weeks

  2. Range of Motion (ROM)

    Cervical range of motion was measured by a standard universal goniometer.

    Time frame: 4 weeks

  3. Functional limitations

    The functional limitation due to mechanical neck pain was evaluated by a neck disability index questionnaire (NDI).

    Time frame: 4 weeks

07

Study locations

1 site
  • Rehabilitation Research Chair
    Riyadh, 11433, Saudi Arabia
08

References and documents

Publications

  • Bharti N, Ahmed H, Hasan S, Iqbal A, Uddin S, Ahamed WM, Ahmad F, Mujtaba MA, Alghadir AH. Efficacy of Scapular Functional and Cervical Isometric Exercises in the Management of Chronic Mechanical Neck Pain: A Randomized Comparative Trial. Pain Res Manag. 2024 Dec 19;2024:5873384. doi: 10.1155/prm/5873384. eCollection 2024. PubMed 39734604 ↗
09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2019 to primary completion in Dec 2019, 3 months.

Of 1,209 non-industry interventional studies with no phase under Chronic Pain, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 39. This study's 3 months is below that.

Counting every sponsor, half of 1,296 studies reached it within 21 months; a quarter within 9 and three quarters within 39.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 7, 2022
First posted
Nov 21, 2022
StartActual
Aug 23, 2019
Primary completionActual
Dec 11, 2019
CompletionActual
Mar 29, 2020
Last update
Nov 23, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 23, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05624021
Collaborators
Majmaah University
Responsible party
AMIR IQBAL (Prinicipal Investigator, King Saud University) — Principal investigator
First posted
Nov 21, 2022
Start date
Aug 23, 2019
Primary completion
Dec 11, 2019
Completion
Mar 29, 2020
Last update
Nov 23, 2022

Study contacts

Amir Iqbal, MPT
study chair · King Saud University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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