Fact CheckerSign in

NCT07181005Completed

The Validity and Reliability of an Improved Paper Grasping Test for Stroke

Application of the Validity and Reliability of the Enhanced Paper Grasping Test in Patients With Stroke

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

The study included volunteer patients diagnosed with stroke who applied to the Neurology Outpatient Clinic at SANKO University Sani Konukoğlu Application and Research Hospital. Patients who met the inclusion criteria were evaluated by Dr Hakan Polat and Physiotherapist Fatma Yılmaz in the application laboratory of the Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, SANKO University. The assessment form prepared by the researchers will be completed face-to-face with the patients. First, the individuals' demographic information and disease information (how many years ago they were diagnosed with stroke, affected side, affected limb, etc.) will be recorded. The mini best test will be used to assess balance and gait. The muscle strength of the plantar flexor muscle groups in the ankle will be assessed using a manual muscle testing device. As fall problems in patients may be related to balance problems, lower limb muscle weakness, particularly in the ankle, and reduced quality of life, these parameters will also be evaluated. Therefore, in our study, while examining the validity and reliability of the modified paper grip test in individuals with stroke, its correlation with these parameters will also be examined. Before the tests are administered, the individuals will be given a practical explanation of how the tests are performed. The individuals will be allowed to rest before the assessments. In the tests, the paper grip test will first be administered by Dr Hakan Polat, followed by the mini best test, the assessment of the strength of the ankle plantar and dorsiflexor muscles. One week after the applications, only the paper grip test will be re-administered by Fzt. Fatma Yılmaz in the same environment. The individuals in this study will be assessed in the same environment in both sessions. In this way, the effect of environmental factors on the patients' performance will be minimised.

Status (registry)
Completed
Study type
Observational
Enrollment
44 (actual)
First submitted
12 Sept 2025
Start date
25 Aug 2025
Primary completion date
10 Sept 2025
Lead sponsor
Sanko University
Diseases
Stroke
NCT number
NCT07181005

What you commit to

  • Study type: Observational
  • Participants enrolled: 44
  • From 25 Aug 2025 to the primary completion date, 10 Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Anyone who has taken any medication that affects their ability to walk or who has suffered an orthopaedic injury within the last month

Other

  • -Pregnant or within the first 3 months after giving birth

Who the study is looking for

  • Participants aged 18-65 with a diagnosis of ischaemic or haemorrhagic stroke
  • Voluntarily participating in the study

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sanko Unıversıty
Coordinator of this site? Confirm its status
GaziantepTurkey (Türkiye)Unknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.