NCT07007923

Brief Summary

This is a cross-sectional obsessional study. This study explores how different sitting conditions affect two important muscles-the diaphragm and the sternocleidomastoid (SCM)-work during breathing exercises. The diaphragm is the main muscle for breathing, while the SCM helps when taking deeper breaths. Understanding how these muscles interact while sitting under various conditions can help improve breathing training techniques. The study's objectives are (1) to investigate the relationship between diaphragm thickness fraction with 4 different sitting conditions during loaded inspiration among healthy adults and (2) To investigate the relationship between SCM activity with 4 different sitting conditions during loaded inspiration among healthy adults. This research will conduct healthy adults, who will be instructed to breathe against resistance provided by the IMT while sitting on four different conditions: a regular chair, a soft pad with feet on the ground, a soft pad with feet on two additional soft pads, and a single soft pad with both feet on one pad. By using ultrasound to measure how thick the diaphragm gets and surface electromyography (sEMG) to track SCM activity, the data will be gathered on how these muscles function under different conditions. The goal is to find out if sitting on unstable surfaces, like soft pads, can enhance diaphragm use compared to a stable chair. These surfaces may change how effectively the diaphragm and SCM work together. This research could lead to better recommendations for inspiratory muscle training (IMT), which helps strengthen these muscles, especially for people with breathing difficulties. By identifying how posture influences muscle recruitment during breathing exercises, hoping to contribute valuable insights that can improve rehabilitation programs for individuals with respiratory conditions.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
45

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

May 10, 2025

Completed
27 days until next milestone

First Posted

Study publicly available on registry

June 6, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

June 19, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 20, 2026

Completed
Last Updated

June 6, 2025

Status Verified

May 1, 2025

Enrollment Period

1 month

First QC Date

May 10, 2025

Last Update Submit

June 3, 2025

Conditions

Keywords

Diaphragmatic thickening fractionSternocleidomastoid musclesinspiratory pressure

Outcome Measures

Primary Outcomes (1)

  • Diaphragmatic thickening fraction

    Diaphragmatic thickening fraction is determined by "(thickness of the diaphragm at end inspiratory - thickness at end expiratory)/thickness at end expiratory". Diaphragmatic thickness will be measured by ultrasonography.

    Through study completion, an average of 1 year

Secondary Outcomes (2)

  • Muscle activation of the sternocleidomastoid muscle

    Through study completion, an average of 1 year

  • Borg's scale

    Through study completion, an average of 1 year

Other Outcomes (1)

  • The Short Form (12) Health Survey

    Through study completion, an average of 1 year

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

aged 18-35 healthy young adults

You may qualify if:

  • aged 18-35 years - No recent thoracic surgery in the past 6 months
  • Absence in history of chronic respiratory illness
  • Able to breathe spontaneously
  • Conscious, able to follow instructions on the use of IMT device

You may not qualify if:

  • with known cardiovascular, pulmonary or musculoskeletal disorders that would limit their functional capacity (E.g. Asthma, COPD)
  • presence with respiratory symptoms over past 2 weeks
  • pregnancy
  • malignancy
  • presence of neurological disorders (e.g. ALS, stroke)
  • PCS/ MCS in SF-12 scores below 50
  • Findings in spirometry suggesting presence of obstructive or restrictive disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hong Kong Metropolitan University Jockey Club Institute of Healthcare

Hong Kong, Hong Kong

Location

Study Officials

  • William Tsang

    Hong Kong Metropolitan University

    STUDY DIRECTOR

Central Study Contacts

Yi On Mak, Bachelor of Physiotherapy

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CROSSOVER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PHD student

Study Record Dates

First Submitted

May 10, 2025

First Posted

June 6, 2025

Study Start

June 19, 2025

Primary Completion

July 31, 2025

Study Completion

April 20, 2026

Last Updated

June 6, 2025

Record last verified: 2025-05

Locations