Scheduled Telephone Intervention for Individuals With Spinal Cord Injury and Their Families (SCILink)

Jeanne Hoffman

Status: Completed

Conditions: Spinal Cord Injury

Treatments: Behavioral: Scheduled Telephone Intervention

Study type: Interventional

Funder types: Other; Other U.S. Federal agency

Identifiers

NCT00693563

32148-G

Details and patient eligibility

About

The purpose of this study is to evaluate whether scheduled telephone intervention with individuals with spinal cord injury (SCI) and their caregivers in the first year following discharge from acute inpatient rehabilitation will reduce rehospitalizations and emergency room visits as well as improve adjustment to SCI.

Full description

This project is a two-group randomized control trial. The control group will receive usual care given to all patients being discharged from acute inpatient rehabilitation following SCI. At 6 months and one year post injury an examiner blinded to group status will contact Control Group participants to collect outcome data.

The Telephone Intervention group (Treatment Group) will also receive their usual care following discharge and a welcome letter, which will include the same information as the Control Group, but also remind them of the up-coming telephone call schedule. Treatment Group participants and their significant others will be contacted by telephone within 24 to 48 hours after discharge and 10 additional times at weeks 1, 2, 4, 6, and months 2, 3, 4, 6, 8, and 10. The frequent early telephone contacts are meant to address early concerns that frequently arise after discharge are expected to last between 30 and 45 minutes. Later phone calls may be brief if no concerns are raised and are expected to address resource needs as well as ongoing questions that arise through the first year after injury. Content of each phone call will be dependent on issues raised by each individual participant and their significant other and/or follow-up on concerns raised in prior phone contacts rather than a specific structured interview. Treatment Group participants will also be contacted at 6 months and one year post injury by the examiner blinded to group status to collect outcome data.

Enrollment: 168 patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• new traumatic SCI
• inpatient acute rehabilitation at the SCI system hospital
• residence in the catchment area at the time of injury

Exclusion criteria

• lack of a telephone
• non-English speaking
• severe psychiatric condition such as psychosis

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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168 participants in 2 patient groups

Control Group

No Intervention group

Description:

The Control Group will receive usual care following discharge from the inpatient rehabilitation unit.

Treatment Group

Experimental group

Description:

Scheduled Telephone Intervention

Treatment:

Behavioral: Scheduled Telephone Intervention