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Development and Clinical Application of a Chinese-Adapted Hand Function Phenotype Assessment Tool

Development and Clinical Application of a Chinese-Adapted Hand Function Phenotype Assessment Tool

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128288
Enrollment
Unknown
Registered
2026-07-17
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Hand Injury (including unilateral hand fractures, tendon ruptures and peripheral nerve injuries)

Interventions

Health Group:None
Hand Injury Group:None

Sponsors

Wuxi 9th People's Hospital affiliated to Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Hand Injury Group: 1. Aged between 18 and 75 years, no gender restrictions; 2. Patients with a clinically and radiologically confirmed diagnosis of hand injury (including: unilateral hand fractures, tendon ruptures and peripheral nerve injuries); 3. Has completed acute-phase treatment (surgery or conservative immobilisation) and is currently in the rehabilitation phase (3–6 months post-injury); 4. The affected upper limb does not present with any significant functional impairment of the shoulder or elbow; 5. Be able to carry out all tests independently; 6. Voluntary participation and signing of the informed consent form. Health Group: 1. Aged between 18 and 75, no gender restrictions; 2. Living in a residential community, fully independent in daily life; 3. No history of hand injuries or surgery; 4. No neurological disorders, severe rheumatic or autoimmune diseases, or uncontrolled severe medical conditions; 5. Be able to understand and cooperate in carrying out all tests; 6. Voluntary participation and signing of the informed consent form.

Exclusion criteria

Exclusion criteria: Hand Injury Group: 1. Severe functional impairment of the contralateral upper limb (e.g. hemiplegia, amputation), which affects auxiliary stabilisation during the test; 2. Diagnosed with complex regional pain syndrome; 3. There is a risk of an unhealed fracture or a re-tear of the tendon; 4. Severe pain (Visual Analogue Scale score > 7) prevented the test from being completed. General exclusion criteria for both the healthy control group and the hand injury group: 1. Presence of cognitive impairment or mental illness that prevents participation in the test; 2. Severe visual impairment (uncorrected) or hearing impairment that affects the ability to understand instructions; 3. Pregnant women (as it may affect stamina and balance); 4. Participants who are concurrently taking part in other interventional clinical trials.

Design outcomes

Primary

MeasureTime frame
Minnesota Test Scores;

Secondary

MeasureTime frame
Physiological functions of the hand;Demographics and Risk Factors;Benchmark indicator;Socio-psychological manifestations;

Countries

China

Contacts

Public ContactZhang Ting

Wuxi 9th People's Hospital affiliated to Soochow University

ting13151592182@163.com+86 13506187116

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026