Supporting Patient Decisions About UE Surgery in Cervical SCI

At present, there is limited information that provides the exact time course and probability
of gain in specific function (such as hand function) that might help patients and clinicians
make decisions regarding novel and time-sensitive surgical treatment options.

Understanding the pros and cons of any surgical intervention, especially in the setting of
complex and often incomplete information, is challenging. Ultimately, this project will
create a decision support intervention (DSI) that can be used to help clinicians and people
living with cervical level SCI and their caregivers. It will be most useful to those with
acute or sub-acute injury (< 1year after SCI) for both military personnel and the general
public. Clinicians and patients will have evidence to help them make decisions about
treatments to improve upper extremity function.

In such a manner, patients can make more well-informed choices that are consistent with their
values, needs and goals.

CERVICAL SPINAL CORD INJURY PARTICIPANTS

Inclusion criteria:

- Adult subjects (≥18 years and < 80 years) with cervical level SCI ASIA A, B or C
(minimum 6 months and maximum 20 years post-injury).

Exclusion criteria:

- Patient who chooses simultaneous tendon and nerve transfer procedure (this would
preclude separation of the influence of one surgery compared to the other)

- Patient has ASIA D status (these patients may have progressive return of functionally
useful motor function below the level of the SCI and would not routinely be offered
acute surgical intervention and their experiences are less-relevant to the target
patient population).

CAREGIVER PARTICIPANTS

Inclusion criteria:

- At least 18 years of age

- Able to answer questions about the primary participant's experiences with cervical
spinal cord injury

Exclusion criteria:

- The caregiver/spouse declines to participate in the study. Note: Caregiver
participation is preferred, but not required, for SCI participant enrollment.