Surgery Clinical Trial
— OI-DBTOfficial title:
Dialectical Behavioral Therapy in High Risk OrthopaedicTrauma Patients
NCT number | NCT03776929 |
Other study ID # | D18154 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2020 |
Est. completion date | December 2020 |
Verified date | March 2020 |
Source | Dartmouth-Hitchcock Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Psychological factors can affect the experience of pain and functional recovery from orthopedic injury. The purpose of this study is to examine the effect of brief Dialectical Behavior Therapy (DBT), a form of psychotherapy, on changing thoughts, feelings, and behaviors that can cause problems in daily living and interfere with recovery from orthopedic injury in patients who are at high risk for chronic pain and disability.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2020 |
Est. primary completion date | December 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - 18 years of age or older - Admitted to Dartmouth-Hitchcock Medical Center with an operatively treated fracture. Exclusion Criteria: - Non-English speaking - Pain Catastrophizing Scale (PCS) score of < 13 - Anticipating hospital length of stay of less than 2 days - Are expected to have severe problems maintaining follow-up and treatment recommendations - Have current or impending incarceration - Are actively psychotic or manic |
Country | Name | City | State |
---|---|---|---|
United States | Dartmouth-Hitchcock | Lebanon | New Hampshire |
Lead Sponsor | Collaborator |
---|---|
Dartmouth-Hitchcock Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change over time in Pain Severity: VAS | Visual Analogue Scale (VAS) Pain scores documented in the patient's medical record. Score Range 0-10. Higher score indicates greater pain. | Baseline, 2 week follow-up, 6-8 week follow-up, 10-14 week follow-up | |
Primary | Number of Opioids Administered | The opioids administered during hospitalization measured in total morphine equivalents | Hospital admission to hospital discharge, approximately 4-7 days | |
Secondary | Change over time in General Health Status | Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health: 10-item measure of physical and mental health. Scale range 0 to 100, mean 50, standard deviation 10. A higher score represents a better outcome. | Baseline, 2 week follow-up, 6-8 week follow-up, 10-14 week follow-up | |
Secondary | Change over time in Psychological Functioning - Depression | Patient Health Questionnaire-9 (PHQ-9): 9-item measure of major depression symptom severity on a 4-point Likert-type scale. Score range 0-27; Higher score indicates more severe depressive symptoms. | Baseline, 2 week follow-up, 6-8 week follow-up, 10-14 week follow-up | |
Secondary | Change over time in Psychological Functioning - PTSD | PTSD Checklist for DSM-5 (PCL-5): 20-item measure of DSM-5 PTSD symptom severity on a 5-point Likert-type scale. Scale range 0-80. Higher score indicates more severe PTSD symptoms | Baseline, 2 week follow-up, 6-8 week follow-up, 10-14 week follow-up | |
Secondary | Change over time in Pain Anxiety: PASS-20 | Pain Anxiety Symptoms Scale (PASS-20): 20-item measure of pain anxiety on a 6-point Likert-type scale. Scale range 0-100. Higher score indicates more pain-related anxiety | Baseline, 2 week follow-up, 6-8 week follow-up, 10-14 week follow-up | |
Secondary | Change over time in Pain Interference: BPI-SF | Brief Pain Inventory-Short Form (BPI-SF): 9-item measure of pain severity and impact of pain on daily functions. This is a 10-point scale with 0 being the best possible score, meaning "no pain", and 10 being the worst possible score, meaning "pain as bad as you can imagine". | Baseline, 2 week follow-up, 6-8 week follow-up, 10-14 week follow-up |
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