NCT05586685

Brief Summary

the study aims to investigate the effectiveness of diaphragmatic release on upper crossed syndrome

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 15, 2022

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 19, 2022

Completed
5 months until next milestone

Study Start

First participant enrolled

March 20, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 20, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 20, 2023

Completed
Last Updated

March 23, 2023

Status Verified

March 1, 2023

Enrollment Period

1 month

First QC Date

October 15, 2022

Last Update Submit

March 22, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • chest expansion with tape measurement

    using tape to measure chest expansion during inspiration and expiration at axillary level and at the level of T10

    up to four weeks

Secondary Outcomes (1)

  • pain intensity with pain numerical scale scale

    up to four weeks

Study Arms (2)

GroupA diaphragmatic release + conventional

EXPERIMENTAL

Group A: diaphragmatic release +conventional The patients will be positioned in the supine position. The therapist stood at the head of the patient contact thoracic cage and ask the patient to take inspiration and move laterally then ask the patient to expire. conventional Subjects will form the letter 'Y' with their arms then they will flex their elbows and move into a position of shoulder extension so that their arms will form the letter 'w L to Y Exercise: Subjects will begin with arms abducted to 90° and elbows flexed to 90° Chin tucks: Subjects will length the neck by pushing the chin into the table in an entirely posterior motion stretch the pectoral area from the supine lying position

Other: effect of diaphragmatic release on upper crossed syndrome

Group B: conventional

EXPERIMENTAL

Group B: conventional posture correction exercises Subjects will form the letter 'Y' with their arms then they will flex their elbows and move into a position of shoulder extension, so that their arms will form the letter 'w L to Y Exercise: Subjects will begin with arms abducted to 90° and elbows flexed to 90° Chin tucks : Subjects will length the neck by pushing the chin into the table in an entirely posterior motion stretch pectoral area from supine lying position

Other: effect of diaphragmatic release on upper crossed syndrome

Interventions

The patients will be positioned in the supine position. The therapist stood at the head of the patient.therapist make manual contact of ribs and ask patient to inspire the move ribs laterally and then expire conventional exercise Subjects will form the letter 'Y' with their arms then they will flex their elbows and move into a position of shoulder extension, so that their arms will form the letter 'w L to Y Exercise: Subjects will begin with arms abducted to 90° and elbows flexed to 90° Chin tucks : Subjects will length the neck by pushing the chin into the table in an entirely posterior motion stretch pectoral area from supine lying position

Group B: conventionalGroupA diaphragmatic release + conventional

Eligibility Criteria

Age17 Years - 22 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Age ranged from 17 to 22 years .
  • Body Mass Index from 20 to 25 kg/m².
  • All participants have an intensity of neck pain on VAS (4-8) (moderate cases).
  • The subjects were chosen from both sexes.
  • All participants have kyphosis angle ≥42°
  • All participants have mechanical neck pain and FHP (craniovertebral angle CVA \< 49).

You may not qualify if:

  • Malignancy
  • Fractures of the cervical spine
  • Cervical radiculopathy or myelopathy
  • Vascular syndromes such as vertebrobasilar insufficiency
  • Rheumatoid arthritis
  • Neck or upper back surgery
  • Taking anticoagulants
  • Local infection
  • Whiplash injury

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Kyphosis

Condition Hierarchy (Ancestors)

Spinal CurvaturesSpinal DiseasesBone DiseasesMusculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
the patients and investigator do not know the groups receive treatment
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
teaching assistant at basic science department, faculty of physical therapy egyptian chinese university

Study Record Dates

First Submitted

October 15, 2022

First Posted

October 19, 2022

Study Start

March 20, 2023

Primary Completion

April 20, 2023

Study Completion

April 20, 2023

Last Updated

March 23, 2023

Record last verified: 2023-03