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Effects of Thumb Manipulation on Hand Grip Strength, Function, and Sensation

The Effects of Thumb Manipulation on Hand Grip Strength, Hand Function, and Sensory Parameters

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07068698
Acronym
THUMBFUN
Enrollment
60
Registered
2025-07-16
Start date
2025-07-06
Completion date
2025-09-06
Last updated
2025-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hand Function in Healthy Individuals, Hand Grip Strength, Hand Sensory Function, Sensory Function, Thumb Manipulation

Keywords

Thumb manipulation, Chiropractic, Hand grip strength, Hand function, Healthy individuals

Brief summary

This randomized controlled study will aim to investigate the effects of thumb manipulation on hand grip strength, function, and sensation in healthy individuals. A total of 60 volunteers aged between 18 and 50 years will be recruited from Ortadağ Special Education and Rehabilitation Center. Participants will be randomly assigned to either a chiropractic manipulation group (n=30) or a control group (n=30), with an equal distribution of males and females in each group. The intervention group will receive thumb manipulation twice weekly for 4 weeks, while the control group will not receive any intervention. Outcome measures will include two-point discrimination (assessed with a discriminator), hand grip strength (measured using a dynamometer), pinch strength (evaluated with a pinch meter), and hand function (measured by the Duruöz Hand Index). Statistical analyses will be performed with a significance level set at p\<0.05. It is expected that participants in the manipulation group will show greater improvements in all measured parameters compared to the control group, suggesting a positive effect of thumb manipulation on hand-related sensorimotor functions in healthy individuals.

Detailed description

This study will be designed as a randomized controlled clinical trial to evaluate the effects of thumb manipulation on hand grip strength, functional ability, and sensory parameters in healthy individuals. Sixty volunteers aged between 18 and 50 years will be recruited from Ortadağ Special Education and Rehabilitation Center. After anthropometric assessments, participants will be randomly assigned into two groups: a chiropractic manipulation group (n=30) and a control group (n=30), with equal numbers of males and females in each group. The intervention group will undergo thumb manipulation performed by a trained physiotherapist twice a week for four weeks. The control group will not receive any intervention during this period. All participants will be evaluated at baseline, at the end of the 4-week intervention, and at follow-up. Outcome measures will include: Hand grip strength, measured using a hand dynamometer, Pinch strength, assessed with a pinch meter on the thumb, index, and middle fingers, Two-point discrimination, evaluated on the thumbs using a discriminator tool, Hand function, assessed using the Duruöz Hand Index. This study will aim to determine whether a short-term thumb manipulation protocol can lead to measurable improvements in sensory and motor functions of the hand in a healthy population. The findings may provide a basis for future research involving clinical populations with hand dysfunction.

Interventions

OTHERThumb Manipulation

This intervention consists of chiropractic manipulation techniques applied specifically to the thumb joint. The manipulation will be performed by a trained physiotherapist twice weekly for 4 weeks. The procedure aims to improve thumb joint mobility, hand grip strength, sensory function, and overall hand function. Each session includes standardized manual therapy maneuvers targeting the thumb's range of motion and soft tissue mobility without the use of any devices or medications. The intervention differs from other manual therapies by focusing solely on the thumb region.

Sponsors

SEFA HAKTAN HATIK
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

The outcome assessors will be blinded to the group assignments to reduce measurement bias. Participants will be aware of their group allocation due to the nature of the intervention (the control group does not receive any treatment). The care providers performing the manipulation will not be blinded.

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged between 18 and 50 * Willing to participate in the study * Have signed the informed consent form * Able to use verbal and written communication skills

Exclusion criteria

* Having contraindications that may prevent manipulation * Having a history of congenital or acquired orthopedic or neurological conditions affecting the upper extremity * Having a history of rheumatological diseases * Having a history of trauma or surgery affecting the upper extremity

Design outcomes

Primary

MeasureTime frameDescription
Duruoz Hand IndexT0 (Baseline, before intervention), T1 (Week 2 of intervention), and T2 (Week 4, end of interventionThe Duruöz Hand Index is a validated self-reported questionnaire used to assess hand function and disability in daily activities. It includes 18 items covering various tasks such as dressing, hygiene, kitchen activities, and carrying objects. Each item is scored on a scale from 0 (no difficulty) to 5 (unable to perform), with higher scores indicating greater hand disability.
Two-Point Discrimination TestT0 (Baseline, before intervention), T1 (Week 2 of intervention), and T2 (Week 4, end of intervention)The Two-Point Discrimination Test is used to evaluate sensory perception and tactile acuity. It measures the smallest distance at which two points of contact can be perceived as separate. In this study, the test will be applied to the thumb (right and left) using a standardized discriminator tool. Lower discrimination distances indicate better sensory perception. The test provides objective data on changes in cutaneous sensory function.
PinchmeterT0 (Baseline, before intervention), T1 (Week 2 of intervention), and T2 (Week 4, end of intervention)Pinch strength will be measured using a standardized pinchmeter to assess lateral, palmar, and tip-to-tip pinch strength in the thumb, index, and middle fingers of both hands. The test will provide quantitative data on fine motor strength and thumb function. Higher values indicate increased pinch strength. The measurement will be used to evaluate the effect of thumb manipulation on hand function.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSEFA H HATIK, Asst. Prof.
haktanhtk@gmail.com+905058761553
Backup ContactOMER D KIZIL, PhD.
omerdiclekizil@gmail.com+905415233691

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026