NCT06119399

Brief Summary

The purpose of the study is to investigate if there is any difference between effect of diaphragmatic doming versus breathing exercises on ventilatory function and core endurance in patients with chronic neck pain

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2022

Typical duration for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2022

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

October 28, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 7, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2024

Completed
Last Updated

August 12, 2024

Status Verified

August 1, 2024

Enrollment Period

1.9 years

First QC Date

October 28, 2023

Last Update Submit

August 8, 2024

Conditions

Keywords

Chronic Neck Pain

Outcome Measures

Primary Outcomes (6)

  • Endurance of deep cervical flexors

    Endurance of deep cervical flexors muscles will be measured by the cranio-cervical flexion test using a pressure biofeedback instrument. During the cranio-cervical flexion test, the subject lay in the crook lying position and the pressure biofeedback instrument will be placed under the neutral cervical spine below the occiput and inflated up to 20 mmHg. The subjects will perform this movement at 5 different pressure levels, i.e., 22, 24, 26, 28, and 30 mmHg. Each level will be supposed to be held for 10 s, and the test will be terminated if they were unable to hold the position for 10 s at any level or if the maximum level was achieved (30 mmHg).

    6 weeks

  • Forced expiratory volume in the first second (FEV1)

    Forced expiratory volume in the first second (FEV1) is one of ventilatory function test parameters, measured using Spirometry, Model SpirOx plus (by Meditech company-China) The forced expiratory volume in 1 second (FEV1) is the volume of air (in liters) exhaled in the first second during forced exhalation after maximal inspiration.

    6 weeks

  • Forced vital capacity (FVC).

    Forced vital capacity (FVC) is one of pulmonary function test parameters, measured using Spirometry, Model SpirOx plus (by Meditech company-China) Forced vital capacity (FVC) is the volume of air that can forcefully expired from the lungs following maximum inspiration, it is measured in liters.

    6 weeks

  • Peak expiratory flow rate (PEFR)

    Peak expiratory flow rate (PEFR) is the maximal flow (or speed) achieved during the maximally forced expiration initiated at full inspiration, measured in liters per second. Peak expiratory flow rate (PEFR) as a pulmonary function, is measured using Spirometry, Model SpirOx plus (by Meditech company-China)

    6 weeks

  • Neck Disability Index (NDI)

    Neck function is assessed using the self-reported Neck Disability Index (NDI), which is a valid and reliable test for measuring neck disability. The NDI consists of 10 items referring to daily activities (work, lifting, driving, sleeping, reading, headaches, recreation, concentration, personal care, and pain intensity). Each item (ranging from 0 to 5, with a score of 0 for no pain and no limitation and a score of 5 for maximum pain and limitation). The total maximum score is 50.

    6 weeks

  • Visual Analogue Score for pain intensity

    Visual Analogue score is a measure of pain severity, it is assessed by the self-reported Visual Analogue Scale (VAS). The Visual Analogue Scale evaluates the intensity of pain. It consists of a 10 cm line, that has two end points, where 0 represents "no pain at all" while 10 indicates "most severe pain". Every patient is asked to rate his/her level of pain by placing a mark on the line. Use a ruler to measure the distance in centimetres from the 'no pain' (or zero) to the current pain mark. This provides pain intensity score out of 10.

    6 weeks

Secondary Outcomes (1)

  • FEV1/FVC ratio

    6 weeks

Study Arms (2)

Breathing Exercises Plus Conventional Exercise Program for Chronic Neck Pain

EXPERIMENTAL

Subjects will receive conventional exercise program for Chronic Neck Pain in addition to breathing exercises (diaphragmatic and pursed lip breathing) for (three sessions per week for six weeks).

Other: Diaphragmatic Breathing ExerciseOther: Pursed Lip Breathing ExerciseOther: Conventional exercise program for chronic neck pain

Doming of the diaphragm plus Conventional Exercise Program for Chronic Neck Pain

EXPERIMENTAL

Patients in this arm will receive conventional physiotherapy treatment for Chronic Neck Pain in addition to doming of the diaphragm (three sessions per week for six weeks).

Other: Doming of the diaphragmOther: Conventional exercise program for chronic neck pain

Interventions

Diaphragmatic breathing exercise will be taught by placing the subject comfortably positioned with either therapist or the patient's hand directed over the abdominal area and instructing the subjects to focus on an outward movement of the abdominal area throughout inspiration and an inward movement of the abdominal area during expiration. (4 sets, and as each set had 4 complete breathing breaks, these exercises will be conducted for 3 days a week for 6 weeks)

Breathing Exercises Plus Conventional Exercise Program for Chronic Neck Pain

Pursed lip breathing exercises will be performed by necessitating the subjects to inhale through their nose and then exhaling slowly for a period of 4-6 s by pursing the lips

Breathing Exercises Plus Conventional Exercise Program for Chronic Neck Pain

* The physiotherapist places the thumbs just inferior to the patient's lower costal margin and xiphoid process with the thumbs pointing cephalad. * The patient is instructed to take a deep breath and exhale. On exhalation, the physiotherapist's thumbs follow the diaphragm, which permits the thumbs to move posteriorly. * The patient is instructed to inhale, and the physiotherapist gently resists this motion. * The patient is instructed to exhale, and the physiotherapist gently follows this motion posteriorly and cephalad, as the thumbs are now beneath the costal margin and xiphoid process. * The patient inhales as the physiotherapist maintains pressure on the upper abdomen and then, on repeated exhalation, encourages further cephalad excursion. * This procedure is repeated for three to five respiratory cycles until the diaphragm domes easily at the end of exhalation.

Doming of the diaphragm plus Conventional Exercise Program for Chronic Neck Pain

Patients will perform three repetitions of stretching exercises for neck flexor, extensor, lateral flexor, and rotator for 30 seconds as warm-up and cool-down exercises, to relieve tension on each side of the neck. Then cranio-cervical flexion exercise will be started using feedback from an air-filled pressure sensor placed behind the neck. Subjects will lay in the crook lying position. The pressure biofeedback unit will be placed below the occiput and inflated up to a baseline pressure of 20 mmHg. The subjects will be instructed to perform head-nodding action to progressively target 5 pressure levels (hold 10 seconds with brief rest periods between each contraction 3-5 seconds). This includes 3 sets in a session for 10 repetitions each with 2 minutes of rest between sets and 3days a week for 6 weeks.

Breathing Exercises Plus Conventional Exercise Program for Chronic Neck PainDoming of the diaphragm plus Conventional Exercise Program for Chronic Neck Pain

Eligibility Criteria

Age20 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patient has chronic neck pain (for more than 3 months)
  • Their age ranged from 20 to 30 years old
  • Their body mass index ranged from (18.5 -29.9) kg/m2
  • Poor results on the cranio-cervical flexion (CCF) test using a pressure biofeedback instrument.

You may not qualify if:

  • History of respiratory disease and Clinical signs of a severe cardiac event.
  • Severe psychiatric or cognitive impairment
  • Tumor and Spinal fractures
  • Spinal cord compression that required urgent surgery
  • Current or past Smokers
  • Obese (BMI \>30) or underweight (BMI ˂18.5)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Outpatient Clinic; Faculty of Physical Therapy, Badr University in Cairo.

Cairo, Badr, Egypt

Location

Outpatient clinic, Faculty of physical therapy, Cairo University.

Giza, Dokki, Egypt

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Eman NE Sayed, M.Sc.

    Assistant Lecturer, dept of internal medicine & geriatric, Badr University in Cairo.

    PRINCIPAL INVESTIGATOR
  • Mina AG Elias, Dr.

    Lecturer, dept of internal medicine & geriatric, Badr University in Cairo.

    STUDY CHAIR
  • Hany E Obaya, Ass.Prof.Dr

    Dept of PT for Cardiovascular/Respiratory Disorder & Geriatrics, Faculty of PT, Cairo Univ.

    STUDY DIRECTOR
  • Asmaa M Sharabash, Dr.

    Dept of PT for Cardiovascular/Respiratory Disorder & Geriatric, Faculty of PT, Cairo Univ.

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Lecturer of Internal Medicine and Geriatric, Faculty of Physical Therapy, Badr University in Cairo.

Study Record Dates

First Submitted

October 28, 2023

First Posted

November 7, 2023

Study Start

March 1, 2022

Primary Completion

January 31, 2024

Study Completion

May 31, 2024

Last Updated

August 12, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations