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The effectiveness of therapeutic craft-making activities in treating lower third forearm fracture: a randomized controlled trial

The effectiveness of therapeutic craft-making activities in treating lower third forearm fracture: a randomized controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000150741
Enrollment
38
Registered
2022-01-28
Start date
2021-07-12
Completion date
2023-11-02
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

Upper limb fracture is conventionally treated using splint, standard modalities, and soft tissue manipulation which offer little psychological benefits. Craft, as the first therapeutic tool used by occupational therapist (OT) has played a significant role since the early history of the profession. Craft can effectively intervene both physical and psychological conditions by providing motivation and foster feelings of satisfaction and hope; and regulate psychophysiological and emotional affects by lowering pain and anxiety. OT that works in the hand therapy field has reduced the use of craft as an intervention due to the lack of documentation and inadequate research. This study aims to determine the benefits of therapeutic craft in addressing the disability, physical impairment and the psychological impact after lower third forearm fracture. This study hypothesised that patients who received therapeutic craft-making session will have greater reduction in disability and post-traumatic stress as well as greater improvement in physical performance. This is a randomized control trial study where participant will be randomly allocated to the control group and intervention group. Patients that undergone surgical treatment for their wrist fracture will be recruited into this study after 2 weeks post-surgery. However, patient with rheumatoid arthritis, multiple limbs or bodily fractures, carpal bone involvement, associated peripheral nerve or/and tendon injury and patient with history of cognitive impairment or psychological condition will be excluded. Participants will undergo 2 therapy sessions per week for 6 weeks (12 sessions). Assessment will be done prior to the commencement of the first therapy session and after the 12th session. Assessment of the disability and post-traumatic stress will be done using questionnaire while physical performance will be assess using clinical assessment tools.

Interventions

Participants in the intervention group will undergo a an extra 10-15 minutes therapeutic craft-making session after receiving standard care treatment. The therapeutic craft-making session will be a one-to-one session, conducted by the researcher with minimum 5 years of experience in hand rehabilitation. The intervention will be commenced after 2-4 weeks post-surgery. Intervention will be delivered twice a week for 6 weeks, with a total of 12 sessions. The researcher will record the participant's

Participants in the intervention group will undergo a an extra 10-15 minutes therapeutic craft-making session after receiving standard care treatment. The therapeutic craft-making session will be a one-to-one session, conducted by the researcher with minimum 5 years of experience in hand rehabilitation. The intervention will be commenced after 2-4 weeks post-surgery. Intervention will be delivered twice a week for 6 weeks, with a total of 12 sessions. The researcher will record the participant's attendance for each session. The therapeutic craft-making session will be conducted in a separate room within the Hand and Upper Limb Centre. Participants will perform crafts including air-dry clay art, quilling, batik painting, origami, threading beads, card making, cloth stamping, wooden frame design, sewing, perler beading, braiding, and soap making. Materials that will be used in the intervention are air-dry clay, papers, cloth, cloth dyes, beads, elastic threads, popsicles sticks, glue, perler beads, rope, soap, fragrance, and soap dye.

Sponsors

Universiti Kebangsaan Malaysia (The National University of Malaysia)
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients with lower third forearm fracture involving individual or combined distal radius, distal ulna, distal radioulnar, radiocarpal joint that undergo open reduction internal fixation (ORIF)

Exclusion criteria

Patient with rheumatoid arthritis, multiple limbs or bodily fractures, carpal bone involvement, associated peripheral nerve or/and tendon injury and patient with history of cognitive impairment or psychological condition

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 8, 2026