NCT03032341

Brief Summary

The purpose of this research study is to find out if mobility (the ability to move around) can be reliably assessed by having the family or care giver caregiver take a video based test for the patient. If this study shows that mobility can be assessed by family or caregiver, this information can be used in situations where mobility cannot be measured directly in patients. A total of 60 patients and 60 family/caregivers at Wake Forest Baptist Medical Center will take part in this study. Patients physical function will be assessed using a test that uses short movie clips to assess mobility. Patients will be asked to watch ten short (\~10 seconds each) movie clips that describe various tasks such as climbing up hills or walking and estimate if they can perform the tasks. The familymember/caregiver will be also asked to answer the questions on behalf of the patient. The family member/caregiver will be asked to return to take the same test in the next 1-14 days. The patient will be in the study for one day. There is no intervention, this is observational.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
130

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

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

January 17, 2017

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

January 18, 2017

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 26, 2017

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 6, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 6, 2017

Completed
Last Updated

March 19, 2026

Status Verified

December 1, 2017

Enrollment Period

3 months

First QC Date

January 18, 2017

Last Update Submit

March 16, 2026

Conditions

Keywords

mobility assessment tool

Outcome Measures

Primary Outcomes (1)

  • Change in MAT-sf score between patients and surrogates

    Investigators will measure the compatibility between patients-surrogates mobility using MAT-sf.

    1-14 days

Study Arms (2)

Patient group

20 patient in poor mobility group (MAT-sf \< 51.38 in men and \<45.61 in women), mid-mobility group (51.38\< MAT-sf≤65.5 in men and 45.61≤MAT-sf\<54.02) and high mobility group (MAT-sf\>65.5 in men and MAT-sf\>54.02 in women) for a total of 60 patients.

Surrogate group

A family member/caregiver that attends visits with the patient and will be asked to answer the Mobility Assessment Test questionnaire on behalf of the patient at the initial visit and the follow up visit 1-14 days later.

Eligibility Criteria

Age70 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

60 patients being seen in the post operative assessment clinic will be asked to complete the Mobility Assessment Tool. A family member/caregiver of each patient will be asked to complete the test on the behalf of the patient at the same visit and asked to complete again 1-14 days later.

You may qualify if:

  • Patients aged 70 years and older being seen at the PAC;
  • Patients who have caregiver or family who meet the criteria for surrogate as above;
  • Patients scheduled for elective surgical procedures.

You may not qualify if:

  • Patients who have a language barrier which will prohibit them from understanding the questionnaire and directions connected to the use of the MAT-sf;
  • Patients who are not able to sign their own surgical consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Wake Forest University Health Sciences

Winston-Salem, North Carolina, 27157, United States

Location

MeSH Terms

Conditions

Mobility Limitation

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Sunghye Kim, MD

    Wake Forest University Health Sciences

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 18, 2017

First Posted

January 26, 2017

Study Start

January 17, 2017

Primary Completion

April 6, 2017

Study Completion

April 6, 2017

Last Updated

March 19, 2026

Record last verified: 2017-12

Data Sharing

IPD Sharing
Will not share

Locations