NCT07218614

Brief Summary

The goal of this study is to determine if manual therapy can improve thoracic spinal posture and pulse oximetery in individuals who use e-cigarettes. The main questions the study aims to answer are:

  • Is there an immediate improvements in thoracic posture
  • Is there immediate improvements in pulse oximetery Research will compare an experimental group and a control group to examine the effects.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
0mo left

Started Oct 2025

Shorter than P25 for not_applicable

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

Study Progress97%
Oct 2025May 2026

Study Start

First participant enrolled

October 15, 2025

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

October 16, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 20, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2026

Expected
Last Updated

October 20, 2025

Status Verified

May 1, 2025

Enrollment Period

6 months

First QC Date

October 16, 2025

Last Update Submit

October 16, 2025

Conditions

Keywords

Thoracic spine, pulse oximetery, mobilzation

Outcome Measures

Primary Outcomes (1)

  • Angle of Thoracic Kyphosis

    Measurement of the thoracic kyphosis will be made both pre and post treatment using excepted normative values (Cobb angle)

    Immediately before and after each intervention

Secondary Outcomes (1)

  • Oxygen Saturation

    immediately before and after intervention

Study Arms (2)

Thoracic Mobilization

EXPERIMENTAL

The intervention group will receive a posterior to anterior directed thoracic mobilization to the mid-thoracic spine to facilitate extension. This will be imparted for a duration of 60 seconds, and this will be repeated for a total of three times. Interventions will be performed in a seated position.

Other: Thoracic Mobilization

Light Touch Contact

SHAM COMPARATOR

The sham treatment will be applied to each subject. The sham treatment of light, non-therapeutic touch will be applied to both scapulae for three minutes. Interventions will be performed in a seated position.

Other: Light Touch Contact

Interventions

The intervention group will receive a posterior to anterior directed thoracic mobilization to the mid-thoracic spine to facilitate extension. This will be imparted for a duration of 60 seconds, and this will be repeated for a total of three times. Interventions will be performed in a seated position.

Thoracic Mobilization

The sham treatment will be applied to each subject. The sham treatment of light, non-therapeutic touch will be applied to both scapulae for three minutes. Interventions will be performed in a seated position.

Light Touch Contact

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Current e-cigarette user Accentuated thoracic kyphosis (Cobb angle \>20 degrees) Age range: at least 18 years old Good overall health

You may not qualify if:

  • History of respiratory disease Recent vertebral fractures Recent spinal surgery Vertebral instability Congenital or acquired thoracic cage deformities Prolonged steroid use Osteoporosis/osteoporosis Inability to provide informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

NYIT

Old Westbury, New York, 11568, United States

Location

Study Officials

  • Teresa M Ingenito, DPT

    New York Institute of Technology

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Teresa M Ingenito, DPT

CONTACT

Mark J Gugliotti, DPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Outcome assessors will not have knowledge of each participant's intervention.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Experimental group will serve as their own control after a one-week washout period.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 16, 2025

First Posted

October 20, 2025

Study Start

October 15, 2025

Primary Completion

April 1, 2026

Study Completion (Estimated)

May 15, 2026

Last Updated

October 20, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

There is no plan to share IPD for this study.

Locations