NCT01876888

Brief Summary

The aims of this study were to perform cultural adaptation of the MedRisk Instrument for Measuring Patient Satisfaction With Physical Therapy Care (MRPS) instrument and provide information regarding the factor structure, group-level reliability, and criterion-referenced validity of the instrument in Turkish speaking patients.

Trial Health

100
On Track

Trial Health Score

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

Enrollment
317

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2011

Status
completed

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

April 1, 2011

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2012

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2013

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

June 7, 2013

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 13, 2013

Completed
Last Updated

June 13, 2013

Status Verified

June 1, 2013

Enrollment Period

1.4 years

First QC Date

June 7, 2013

Last Update Submit

June 12, 2013

Conditions

Cultural Adaptation

Keywords

patient satisfactionphysical therapyMedRisk instrument

Outcome Measures

Primary Outcomes (1)

  • patient satisfaction instrument

    5 minutes

Eligibility Criteria

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

Patients from various regions in Turkey who were receiving outpatient physiotherapy programs.

You may qualify if:

  • All subjects had to be able to read and write in Turkish.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Patient Satisfaction

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Özgen Aras

    T.C. Dumlupınar Üniversitesi

    STUDY DIRECTOR

  • Cigdem Ayhan

    Hacettepe University

    PRINCIPAL INVESTIGATOR

  • Yavuz Yakut

    Hacettepe University

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
15 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

June 7, 2013

First Posted

June 13, 2013

Study Start

April 1, 2011

Primary Completion

September 1, 2012

Study Completion

March 1, 2013

Last Updated

June 13, 2013

Record last verified: 2013-06