NCT03997942

Brief Summary

Purpose of the study; The aim of this study was to investigate the effect of two different exercise programs on joint patency, pain, functionality, kinesophobia and quality of life in upper extremity burn patients. Lütfi Kırdar Training and Research Hospital Burn and Wound Center and unilateral upper extremity burns will consist of individuals aged 18-65 years. 48 burn patients who volunteered to participate in the study will be included in the study. Demographic information of the cases will be recorded. Joint range of motion and pain will be evaluated with the Visual Analogue Scale (VAS) before and after the treatment program. Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire will be used to evaluate upper extremity functions. TAMPA Kinezophobia questionnaire will also be used for kinesiophobia. To evaluate the quality of life, Burn-Specific Health Scale developed for burn patients will be used.

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
48

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2019

Shorter than P25 for all trials

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

Study Start

First participant enrolled

May 1, 2019

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

June 18, 2019

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 25, 2019

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 20, 2019

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2019

Completed
Last Updated

June 25, 2019

Status Verified

June 1, 2019

Enrollment Period

5 months

First QC Date

June 18, 2019

Last Update Submit

June 24, 2019

Conditions

Burn; Arm

Keywords

burn, physiotherapy

Outcome Measures

Primary Outcomes (6)

  • Demographic information

    Demographic information of the cases will be recorded.Age, cause of burn, burn zone, burn percentage will be recorded.

    10 minutes

  • Joint range of motion

    The goniometer will measure the range of motion.

    15 minutes

  • Pain assesment

    Pain will be assessed by visual pain scale.

    5 minutes

  • Functional assesment

    Shoulder-Arm Function Questionnaire will be used to evaluate upper extremity functions.

    15 minutes

  • Fear of Motion

    The Tampa Kinesophobia Questionnaire will be used to assess fear of movement.

    10 minutes

  • Quality of Life Assesment

    A scale specific to burn patients will be used to evaluate the quality of life.(Burn Specific Health Scale)

    15 minutes

Study Arms (3)

proprioceptive neuromuscular facilitation

PNF will be applied to randomly selected patients.

Other: Effect of exercise

Mirror therapy

Mirror therapy will be applied to randomly selected patients.

Other: Effect of exercise

Standart therapy

Standard treatment will be applied to randomly selected patients.

Other: Effect of exercise

Interventions

Effect of exerciseOTHER

Once the data are available, we hope to have information about which of the exercise practices included in the rehabilitation program of acute upper extremity burn patients is more effective.

Mirror therapyStandart therapyproprioceptive neuromuscular facilitation

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Acute Burn Patients

You may qualify if:

  • \- Agreeing to participate voluntarily in the study -

You may not qualify if:

  • T.C. Ministry of Health Kartal Lütfi Kırdar Training and Research Hospital Burn and Wound Center treated patients between the ages of 0-18,
  • Burn patients who refused to participate in the study, - Patients with bilateral upper extremity burns

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Wound and Burn Center

Istanbul, 34865, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Burns

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Officials

  • Mine Seyyah

    DrLutfiKirdar

    STUDY CHAIR

Central Study Contacts

Mine Seyyah, Msc

CONTACT

0905333566908mine-fzt@hotmail.com

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
6 Months
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Msc Physiotherapist

Study Record Dates

First Submitted

June 18, 2019

First Posted

June 25, 2019

Study Start

May 1, 2019

Primary Completion

September 20, 2019

Study Completion

December 15, 2019

Last Updated

June 25, 2019

Record last verified: 2019-06

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)