NCT04749472

Brief Summary

Participants will be measured with motion monitor system while using 6 different slings. Measurement order will be randomized, and 5 minutes resting period will be given prior measurement. Scapula, humerus and thorax positions will be recorded in resting position and then with slings.

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
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2021

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

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

February 7, 2021

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 11, 2021

Completed
4 days until next milestone

Study Start

First participant enrolled

February 15, 2021

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 12, 2022

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2022

Completed
Last Updated

February 11, 2021

Status Verified

February 1, 2021

Enrollment Period

1.6 years

First QC Date

February 7, 2021

Last Update Submit

February 7, 2021

Conditions

Shoulder InjuriesSurgery

Keywords

RehabilitationShoulder SurgeryPostoperative

Outcome Measures

Primary Outcomes (1)

  • Motion Monitor

    Motion monitor device was used to analyze 3D positions of the arm, shoulder, scapula and thorax.

    During rest position without and with different slings for 5 seconds.

Study Arms (1)

Study Group

EXPERIMENTAL

Participants received intervention.

Other: Sling

Interventions

SlingOTHER

Participants wore six different shoulder slings in a randomized order.

Study Group

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may not qualify if:

  • Having a shoulder surgery
  • Having scapular dyskinesis,
  • Having shoulder pain,
  • Having any disease that could affect posture and/or shoulder (such as scoliosis)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hacettepe University

Ankara, 06100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Shoulder Injuries

Interventions

Suburethral Slings

Condition Hierarchy (Ancestors)

Wounds and Injuries

Intervention Hierarchy (Ancestors)

Prostheses and ImplantsEquipment and Supplies

Central Study Contacts

Elif Turgut, Assoc Prof.

CONTACT

+905442645600elif.turgut.pt@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: Participants wore different sling in a randomized order.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
assistant professor

Study Record Dates

First Submitted

February 7, 2021

First Posted

February 11, 2021

Study Start

February 15, 2021

Primary Completion

September 12, 2022

Study Completion

December 20, 2022

Last Updated

February 11, 2021

Record last verified: 2021-02

Locations

TU(1)