ClinicalTrials.gg
RecruitingNCT06935812Updated May 19, 2026

Comparison of the Effects of Bimanual, Finger and VR Exercises in PwMCI

An interventional study of Bimanual Exercise and Finger Exercise in Mild Cognitive Impairment, sponsored by Eastern Mediterranean University. Recruiting at 1 site in Cyprus. Open to participants aged 50 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-19.

Sponsored by Eastern Mediterranean University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2025; still recruiting 1 year 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
106
Allocation
Randomized
Ages
50 Years to 75 Years
Sex
All
01

Study summary

Mild Cognitive Impairment (MCI) is defined as an impairment in a single cognitive function, usually memory, other than normal cognitive decline with age, that does not fulfil dementia criteria. Finger movements have been shown to stimulate the sensory-motor and cognitive parts of the cerebral cortex, as well as the supplementary motor area, Broca's area, premotor cortex, and prefrontal cortex, all of which contribute to movement skills. Asymmetrical hand and finger movements done concurrently were proven to improve cognitive processes and cerebral blood flow more than movements performed with one hand.

Read the detailed description

Cognitive impairment is one of the most pressing healthcare problems of the 21st century. Mild cognitive impairment (MCI) has been defined as a disorder in a single cognitive function; usually, memory is impaired to an extent greater than anticipated for age, yet the patient does not meet the criteria for dementia. MCI, known as a risk factor for the early stage of dementia, constitutes a risk factor for Alzheimer's Disease (AD) and is also known as the prodromal syndrome of AD. MCI affects 3%-22% of people over the age of 65, depending on demographic characteristics, and persons with MCI (PwMCI) progress to dementia at a rate of 10%-15% every year. Advanced age, low education level, and low cognitive capacity are among the most common risk factors for MCI. Although the pathology of MCI is not completely understood, hippocampal and entorhinal cortex atrophy is defined as a hallmark, and the connectivity of the hippocampus with the prefrontal lobe, temporal lobe, parietal lobe, and cerebellum was found to be lower in PwMCI than healthy controls. PwMCI can be categorized as amnestic and non-amnestic MCI. Individuals with non-amnestic MCI have impairments in other domains than memory, such as attention/executive functions (eMCI), which are frequent and disabling symptoms MCI. It was shown that response inhibition, switching, and cognitive flexibility are selectively impaired, while sustained and divided attention are intact in PwMCI. It has been proposed that executive control and gait share common frontal brain circuitry vulnerable to age-related neuropathology. It is known that cognitive deficits are associated with increased fall risk in community-dwelling older adults, and older adults with higher cognitive impairments are more prone to experience falls. The stepping reaction time variability indicate compromised neural circuitry involved in executive function, gait, and posture and increases the risk of fall in PwMCI.

A promising avenue in this regard is finger or hand exercise, which is rooted in traditional Chinese medicine and grounded in the meridian theory. The meridian theory suggests that specific meridians and acupoints can be stimulated through finger exercises, leading to the promotion of energy flow and restoration of overall balance within the body. While finger exercise has a historical foundation in traditional Chinese medicine, its potential impact on cognitive function has recently gained attention, resulting in several studies investigating its benefits. Notably, two recent randomized controlled trials (RCT) demonstrated that finger exercise improved cognitive performance in both cerebral ischemic stroke (CIS) and mild cognitive impairment (MCI) patients. Despite the promising nature of finger exercises as an effective cognitive intervention highly accessible to older adults, a thorough investigation of their effects is imperative before widespread application.

02

Conditions studied

  • Mild Cognitive Impairment

Keywords

  • Finger Exercise
  • Bimanual Exercise
  • Virtual Reality
  • Processing Speed
  • Cognitive Functions
  • Walking Speed
  • Gross Motor Skills
  • Fine Motor Skills
  • Dual Task
03

In context

Cognitive Dysfunction

3,872 studies on the registry are indexed under Cognitive Dysfunction; 1,119 are open to participants now.

This study's planned enrollment of 106 is above the median of 64 across 2,794 interventional studies indexed under Cognitive Dysfunction.

Browse Cognitive Dysfunction studies →

Lead sponsor

Eastern Mediterranean University is the lead sponsor of 141 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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.

Inclusion criteria

  • Participants who are between 50-75 years of age
  • Individuals diagnosed with MCI by a geriatrician according to criteria,
  • Who has the score between 13-26,
  • Who has the Quick Mild Cognitive Impairment screen score between 48-67,
  • Who has Instrumental Activities of Daily Living Scale score ≥6/8,
  • Who says yes to "Do you have a memory problem?" question,
  • Who can walk independently without using any walking aids

Exclusion criteria

Exclusion Criteria:

  • Participants who have any musculoskeletal disorders that may cause balance and gait disorders,
  • Who have central or peripheral neurological diseases (eg. stroke, Parkinson's disease or polyneuropathies),
  • Who are using psychiatric drugs that may affect psychiatric disease and/or cognitive performance (Using nonsteroidal anti-inflammatory drugs more than three times a week, which may affect cognitive functions, using gingko biloba and antioxidant supplements (for example, coenzyme Q10 and alpha-lipoic acid)),
  • Who has daltonism and
  • Who attends any exercise program last 6 months will not be included in this study.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

MMSE and MoCA

Short tests of memory and thinking, each scored out of 30. Lower scores suggest more difficulty; criteria give a range, either to include people with memory problems or to leave them out.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
106 participants (estimated)

Study arms

  • Experimental
    Bimanual Exercise

    Bimanual Exercise The bimanual exercise group consists of exercises that involve movements in which both hands are used simultaneously. The bimanual exercise group will have 40 minutes of training for 3 sessions per week for 8 weeks.

    Other: Bimanual Exercise

  • Experimental
    Finger Exercise

    Finger Exercise The finger exercise group consists of exercises that involve finger movements. The bimanual exercise group will have 40 minutes of training for 3 sessions per week for 8 weeks.

    Other: Finger Exercise

  • Experimental
    Virtual Reality

    Virtual Reality The virtual reality exercise group consists of hand-tracking game exercises that involve finger movements. The bimanual exercise group will have 40 minutes of training for 3 sessions per week for 8 weeks.

    Other: Virtual Reality

  • No intervention
    Control

    In this group, participants will asses on the first and the last weeks of the program (0. and 8. week).

Interventions

  • OtherBimanual Exercise

    The bimanual exercise group consists of exercises that involve movements in which both hands are used simultaneously. The bimanual exercise group will have 40 minutes of training for 3 sessions per week for 8 weeks.

  • OtherFinger Exercise

    The finger exercise group consists of exercises that involve finger movements. The bimanual exercise group will have 40 minutes of training for 3 sessions per week for 8 weeks.

  • OtherVirtual Reality

    The virtual reality exercise group consists of hand-tracking game exercises that involve finger movements. The bimanual exercise group will have 40 minutes of training for 3 sessions per week for 8 weeks.

06

What researchers measure

Primary outcomes

  1. MoCA

    Montreal Cognitive Assessment Scale: MoCA is a short screening test for Mild Cognitive Impairment and Alzheimer's Disease to measure cognitive functions. The test is administered using pen and paper and takes approximately 10-20 minutes. It has 7 subheadings and these are listed as follows: (1) visuospatial/executive functions (clock drawing and cube copying, tracing test (part B) - 5 points); (2) naming (learning and repeating a list of 5 words - 3 points); (3) memory (5 points for recall); (4) attention (target-orientated clapping - 6 points); (5) language (fluency - 3 points); (6) abstract thinking (similarity between words - 2 points); and (7) orientation (knowledge of day, month, year and place - 6 points). The score range is 0 to 30, with higher scores indicating better performance. Values below 26 points indicate a risk of cognitive impairment and provide information about a possible MCI.

    Time frame: 8 weeks

  2. Cognitive functions-Trail Making Test (A-B)

    Trail Making Test (A-B): Trail Making Test (TMT) is a complex visual screening test with motor components and is sensitive to frontal region functions (12, 13). Motor speed, agility and careful participation are required to be successful in this test. This first version of the IST consists of two parts (forms), A and B. In Part A, the participants will be asked to connect the circles with numbers (1-2-3-4-......) on the test form by drawing a line consecutively and in the correct order. In Part B, the participants will be asked to connect the circles containing numbers and letters (1-A,2-B,3-C- ......) on the test form by drawing a line in a consecutive and correct order in accordance with the order of one number and one letter. The time will be recorded for both A and B tests.

    Time frame: 8 weeks

  3. Cognitive functions-Digit Span Test/Digit Symbol Substitution Test

    Digit Span Test (DST): In the DST, participants will be asked to repeat the read digits in sequence. The test continues with growing digits. Then, in the second part of the test, they will be asked to repeat the spoken digits backwards and the number of correct ones will be recorded. Digit Symbol Substitution Test (DSST): DSST is a test used to evaluate psychomotor performance. The participants will be asked to draw the symbol determined for each number in the boxes left blank for 90 seconds. The total number of correct shapes will be recorded.

    Time frame: 8 weeks

  4. Cognitive Functions-Verbal Fluency Test/Serial Subtraction Test

    Verbal Fluency Test - Phonemic: The participant is asked to count the words starting with the letters we have determined (letters A and S) within 1 minute. The number of correct and incorrect words spoken will be determined. Serial Subtraction Test: The participant is asked to count backwards by subtracting 7 from a number between 200-300 within 1 minute. The number of correct and incorrect counts will be determined.

    Time frame: 8 weeks

Secondary outcomes

  1. Choice Stepping Reaction Time Mat (CSRT)

    Lower extremity reaction time: Step taking reaction time will be evaluated on the Choice Stepping Reaction Time Mat (CSRT) with Flash/response facilitation (stepping as fast as possible in the direction of the lit green arrow) and Inhibitor/response inhibition (staying in place when the purple arrow is lit and stepping with the green arrow). Accordingly, reaction time, movement time and response/operation time (sum of reaction time and movement time) will be evaluated in all tests. Upper extremity reaction time: While the participant is in a sitting position, he/she will be asked to touch the buttons (Blaze Pods) on the table as fast as possible when the light is on and the reaction time will be recorded. The test will be performed separately for right and left extremities.

    Time frame: 8 weeks

Other outcomes

  1. Grip Strength

    Hand held dynamometer: A hand held dynamometer will be used to measure grip strength, which begins to decline with ageing. The participant will sit with the shoulder in adduction, elbow in 90 degree flexion, forearm and wrist in neutral position. The therapist will then place the dynamometer in the hand of the person being tested and ask them to squeeze as hard as possible. The participants will be asked to grasp the grip with all their strength for both hands and the average of the three repetitions will be taken.

    Time frame: 8 weeks

  2. Fine motor skills

    Purdue Pegboard Test: The total duration of the test, including the introduction time, is 5-10 minutes. The materials required are a rectangular pegboard with 25 holes along two rows and a stopwatch. At the end of the application, a total of five different scores will be obtained with measurements such as right hand, left hand, both hands together, combined task and sum of scores. During the application, the person will be asked to insert the nails into the holes and the total number will be calculated after 30 or 60 s depending on the task. Individuals will be given 30 seconds for right hand, left hand and double hand evaluation, while the individual will be given 60 seconds for the evaluation test performed by stacking them one on top of the other with the coordinated movement of both hands, which is called combined movement.

    Time frame: 8 weeks

  3. Gross motor skills

    Box and Block Test: The materials required for the test consist of a stopwatch, a wooden box with a centre compartment and 150 wooden cubes. The total duration of the test is 2-5 minutes. Participants will be asked to pass the cubes one by one from one compartment to the other compartment within 60 seconds and the number of cubes will be noted. This test will be applied separately for both extremities.

    Time frame: 8 weeks

  4. Gait characteristics

    10 Metre Walk Test: The 10 Metre Walk Test will be used to determine walking speed. Within the scope of the test, an area of 10 metres will be determined and the time taken to walk this distance will be recorded. A mobile application (OneStep) will be used to record walking speed. The individuals will be asked to walk a distance of 10 metres by placing the phone in the right pocket of their trousers. Time to perform the test, number of steps, step duration, step length, cadence and walking speed values will be recorded.

    Time frame: 8 weeks

  5. Dual task performance/Walking

    10 Metre Walk-Verbal Fluency Test (10MW-VFT): The phone will be placed in the right pocket of the individuals' trousers and they will be asked to say words starting with the letter "A" aloud while walking a distance of 10 metres. The number of steps, step duration, step length, cadence, walking speed, time to perform the test, and the number of correct and incorrectly spoken words will be recorded. 10 Metre Walk-Serial Subtraction Test: The phone will be placed in the right pocket of the individuals' trousers and while walking a distance of 10 metres, they will be asked to count backwards by subtracting 3 from a randomly selected number between 200-300. The walking characteristics and words will be recorded same as 10MW-VFT.

    Time frame: 8 weeks

  6. Dual task performance/Sitting

    Purdue Pegboard-Verbal Fluency: While performing the Purdue Pegboard test, the patient will be asked to count words starting with the letter 'S' within 30 seconds. The test will be conducted separately for the right and left hand. At the end of the test, the correct answer and the number of sticks will be recorded. Purdue Pegboard-Serial Subtraction Test: During the Purdue Pegboard test, individuals will be asked to count backwards by 3 from a number between 300-400 within 30 seconds. The test will be performed separately for the right and left hand. At the end of the test, the correct answer and the number of sticks will be recorded.

    Time frame: 8 weeks

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2025 (actual). Primary completion is estimated for Sep 2026, 16 months after the start.

Of 1,442 non-industry interventional studies with no phase under Cognitive Dysfunction, half reached primary completion within 27 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 51. This study's planned 16 months is below that.

Counting every sponsor, half of 1,511 studies reached it within 27 months; a quarter within 12 and three quarters within 50.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 1, 2024
First posted
Apr 20, 2025
StartActual
Apr 29, 2025
Primary completionEst.
Sep 24, 2026
CompletionEst.
Sep 24, 2026
Last update
May 19, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06935812
Responsible party
Betül Fatma Bilgin (Research Assistant, Eastern Mediterranean University) — Principal investigator
First posted
Apr 20, 2025
Start date
Apr 29, 2025
Primary completion
Sep 24, 2026 (estimated)
Completion
Sep 24, 2026 (estimated)
Last update
May 19, 2026

Study contacts

Betül Fatma Bilgin, MSc PT
Contact
betulll_96@hotmail.com
3926303011
Gözde İyigün, PhD
Contact
gozde.iyigun@emu.edu.tr
3926303011
Betül Fatma Bilgin, MSc PT
principal investigator · Eastern Mediterranean University
Gözde İyigün, PhD
study director · Eastern Mediterranean University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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