NCT06644222

Brief Summary

Double-crossed syndrome" refers to a specific alignment of overactive and underactive muscles in the neck, chest, and shoulders. AIRROSTI stands for Applied Integration for the Rapid Recovery of Soft Tissue Injuries. This study aims to evaluate the effectiveness of Airrosti exercises combined with TheraBand exercises in reducing pain and disability in the neck and shoulders. TheraBand exercise programs are commonly used to improve muscle activation. However, research on the effectiveness of AIRROSTI combined with TheraBand exercises for treating Double-Crossed Syndrome among smartphone users is limited, and more evidence is needed to support their effectiveness.

Trial Health

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Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
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

October 8, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

October 16, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

December 10, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2025

Completed
Last Updated

May 20, 2025

Status Verified

May 1, 2025

Enrollment Period

1 year

First QC Date

October 8, 2024

Last Update Submit

May 19, 2025

Conditions

Keywords

Double crossed syndromposturesmart phone users

Outcome Measures

Primary Outcomes (1)

  • University of California at Los Angeles Activity Scale

    Pre and post intervention measurement will be taken using University of California at Los Angeles Activity Scale. The minimum score is zero indicating several functional impairments and maximum score is 35 , indicating a normal upper limb activity.

    6 week

Other Outcomes (2)

  • Double Square Test

    6week

  • Numeric Pain rating scale

    6 week

Study Arms (2)

Groupe A

ACTIVE COMPARATOR

Experimental groupe A will receive AIRROSTI exercises for 45 minutes / one session daily for five days per week.

Behavioral: AIRROSTI exercises

Groupe B

ACTIVE COMPARATOR

Group B will receive Thera band exercises for 45 minutes/one session per day for five days per week.

Behavioral: Thera band exercises

Interventions

Group A will receive AIRROSTI exercises for 45 minutes / one session daily for five days per week

Groupe A

Group B will receive Thera band exercises for 45 minutes/one session per day for five days per week.

Groupe B

Eligibility Criteria

Age18 Years - 25 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsFemale with rounded shoulder posture
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • young female participants with rounded shoulder postures. Participants aged between 18 and 25 years. No history of shoulder trauma, current shoulder pathology, thoracic scoliosis, and kyphosis deformity.

You may not qualify if:

  • Participants excluded if they received any other form of medical treatment or have thoracic scoliosis or kyphosis deformity.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Majmaah University

Al Majma'ah, Alriyadh, 11952, Saudi Arabia

RECRUITING

Study Officials

  • Shahnaz Hasan associate Professor, PhD

    Majmaah University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Shahnaz Hasan, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Two intervention groups
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

October 8, 2024

First Posted

October 16, 2024

Study Start

December 10, 2024

Primary Completion

December 15, 2025

Study Completion

December 30, 2025

Last Updated

May 20, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

There is no plan to share, it will be available with principal author and provided upon request.

Locations