Actively Recruiting

Age: 18Years +
All Genders
ID06399614

An Evidenced Based Analytical Study of Occupational Therapy-led Services for Adults Presenting Acutely With a Hand Condition

Led by University of Limerick · Updated on 2025-10-01

150

Participants Needed

5

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Traumatic hand injuries contribute to about one third of acute hospital visits. This research aims to evaluate the effectiveness of occupational therapy-led hand therapy services for adults who come to emergency departments or injury units with hand conditions. The study involves four sites in Ireland, including one without occupational therapy access, providing care as usual for comparison. The goal is to improve care quality and guide future service development for hand injuries. Participants at sites with occupational therapy access will be referred to specialized hand therapy clinics where therapists will offer treatments such as customized splinting, targeted exercises, swelling and scar management, desensitisation, education, and occupation-based activities. Those at the comparison site will receive usual care, which may include nursing and medical care, wound care, off-the-shelf orthoses, education, and referrals. Treatments are personalized and based on established protocols. The study will track outcomes at initial contact, 8 weeks, and 6 months. Participants will complete assessments measuring function, pain, quality of life, and occupational competence using standardized tools like QuickDASH, EuroQoL EQ-5D-5L, Occupational Self Assessment, and pain rating scales at baseline, 8 weeks, and six months. Researchers will analyze demographic, clinical, and process outcomes, aiming to identify patient, organizational, and societal benefits. The study runs until November 2025 and hopes to support evidence-based occupational therapy services for hand injuries.

CONDITIONS

Brief Title

Occupational Therapy-led Services for Adults Presenting Acutely With a Hand Condition

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years of age and older
  • Adults presenting with an injury and/or condition of their hand and/or forearm that inhibits function, including fractures, tendon and soft tissue injuries, digital nerve injuries, or carpal tunnel injury
Not Eligible

You will not qualify if you...

  • Patients under 18 years of age
  • Patients with complex medical issues alongside hand injury requiring alternative care pathways or urgent hospital transfer
  • Other exclusions based on team capacity and expertise at the service's discretion

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Occupational Therapy-led Hand Therapy Service or Care as Usual

Duration - Individualised to patient recovery stages

Participants receive either occupational therapy-led hand therapy interventions or care as usual after presenting acutely with a hand condition. Interventions may include splinting, exercises, edema and scar management, desensitisation, education, and functional task completion, or standard nursing and medical care.

1 baseline visit at initial contact

Follow-up and Outcome Assessments

Duration - 6 months from initial contact

Participants complete outcome measures to assess function, pain, and quality of life at 8 weeks and 6 months after initial contact.

2 follow-up visits at 8 weeks and 6 months

Trial Site Locations

Total: 5 locations

1

Beaumont Hospital

Dublin, Ireland

Actively Recruiting

2

Tallaght University Hospital

Dublin, Ireland

Not Yet Recruiting

3

Galway University Hospital

Galway, Ireland

Not Yet Recruiting

4

Ennis General Hospital - ULHG

Limerick, Ireland

Actively Recruiting

5

Nenagh General Hospital ULHG

Tipperary, Ireland

Actively Recruiting

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Research Team

M

Margo Sheerin

A

Ann-Marie Morrissey, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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