An interventional study of Sensory Training and classical hand therapy in Proprioception, sponsored by Sanko University. Status unknown at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-12-05.
Sponsored by Sanko University · Not applicable, Interventional, and Treatment
The aim of this study is to determine the benefits of sensory training for participants who are included in rehabilitation after carpal tunnel surgery.
605 studies on the registry are indexed under Carpal Tunnel Syndrome; 138 are open to participants now.
This study's planned enrollment of 30 is below the median of 60 across 457 interventional studies indexed under Carpal Tunnel Syndrome.
Browse Carpal Tunnel Syndrome studies →Sanko University is the lead sponsor of 52 studies on the registry; 11 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Other: classical hand therapy
Procedure: Sensory Training
The sensory training group includes sensory-oriented interventions and exercises unlike the other classical hand therapy group.
classical hand therapy
Joint Position Matching
In our study, the wrist joint's range of motion will be evaluated in 2 different directions (flexion / extension and radial / ulnar deviation) for proprioception evaluation. For evaluations of all directions, the individual will be required to bring the wrist to the end of the movement, then to perform half the normal range of motion, while the wrist is in a hanging position from the table edge to allow full movement. The difference between the angular value and the angular value created by the individual will be noted by looking at the angular value on the fixed goniometer.
Time frame: Baseline (First day)
Purdue Pegboard Test
The Purdue Pegboard Test is a neuropsychological test of manual dexterity and bimanual coordination.
Time frame: Baseline (First day)
Activity Limitation
The Patient-Specific Functional Scale is a self-reported, patient-specific outcome measure, designed to assess functional change, primarily in patients presenting with musculoskeletal disorders. The scale was developed by Stratford et al 1995 as a self-report measure of function that could be used in patients with varying levels of independence. It was designed to provide clinicians with a valid, reliable, responsive, and efficient outcome measure that would be easy to use and applicable to a large number of clinical presentations.
Time frame: Baseline (First day)
Health-Related Quality of Life
The EuroQoL-five-dimension (EQ-5D) is one of the most commonly used questionnaires to elicit health state utilities, having both a youth and an adult version. For general populations of adults two versions of the questionnaire have been developed, 3L and 5L, with the latter offering a more detailed description of health status. In order to use the EQ-5D to estimate quality-adjusted life-years, a value set to reflect people's preferences for different health states is needed.
Time frame: Baseline (First day)
Started Jul 2018 (actual). Primary completion is estimated for Mar 2020, 19 months after the start.
Of 257 non-industry interventional studies with no phase under Carpal Tunnel Syndrome, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 27. This study's planned 19 months is above that.
Counting every sponsor, half of 267 studies reached it within 12 months; a quarter within 7 and three quarters within 27.
How these figures are worked out, and which studies are left out of them.
This study is status unknown, as verified in Dec 2019. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Sanko University