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Rehabilitation Programmes for Scapholunate Instability

A Pilot Study to Investigate Two Different Physiotherapy Rehabilitation Programmes, to Treat the Conservatively Managed Scapholunate Instability.

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03839901
Enrollment
2
Registered
2019-02-15
Start date
2017-08-01
Completion date
2018-08-01
Last updated
2019-02-15

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

Conditions

Scaphoid-Lunate Instability, Wrist Sprain, Wrist Strain

Keywords

Scaphoid-Lunate, instability, wrist

Brief summary

Two different exercises approaches were tested in patients with Scapho-Lunate (SL) instability; one to strengthen the tendons in static positions and the other to strengthen the tendons whilst the wrist is moving.

Detailed description

Scapho-Lunate (SL) instability is the most common form of wrist instability, but is complex to diagnose and is often missed entirely. The natural progression of SL instability has been suggested to lead to osteoarthritis. The management of SL instability can be broadly divided into conservative and surgical, with the former being the first option taken by most medical professionals, which primarily involves physiotherapy. The evidence base for physiotherapy management of SL instability is limited; however cadaver research has identified loading some of the wrist tendons may stabilise the scaphoid and lunate.There is currently no research as to whether this clinically makes any difference to the patients symptoms, or how to do it. This research therefore aimed to test the protocol and methods, and act as a platform for larger studies, to investigate this. Two different exercises approaches were tested; one to strengthen the tendons in static positions and the other to strengthen the tendons whilst the wrist is moving.

Interventions

OTHERHome exercise program

Home exercise programme with participants followed up at week 1, 4, 6 and 8.

Sponsors

Bradford Teaching Hospitals NHS Foundation Trust
CollaboratorOTHER_GOV
University of Bradford
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Ages eighteen to sixty, * wrist pain, * confirmed scapholunate ligament disruption on MRA or XR (partial or full), * referred from orthopaedic wrist specialist, * for conservative management, * consent to trial.

Exclusion criteria

* Under eighteen or over sixty years, * previous fracture, * degenerative changes in the wrist, * previous surgery, * complex regional pain syndrome or diagnosis of rheumatological conditions, * no wrist injection in preceding twelve months or other wrist conditions.

Design outcomes

Primary

MeasureTime frameDescription
Grip strength using E-link dynamometerassessed at 0, 4 and 8 weekschange of grip strength from baseline change of 20% in kg considered signifcant

Secondary

MeasureTime frameDescription
numerical rating scaleassessed at 0, 4 and 8 weeksPain scored on a numerical rating scale 0 (no pain) -10 (unbearable pain) Minimally Clinical Important Difference of 20mm
Patient Rated Wrist Evaluationassessed at 0, 4 and 8 weeksUsed Patient Rated Wrist Evaluation PRWE questionnaire (A score of 100 represents the worst functional score, whereas 0 represents no disability) with Minimally Clinical Important Difference of 14 points

Countries

United Kingdom

Outcome results

None listed

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