Project Details
Description
Primary Specific Aim 1: Evaluate the ability of the TMH intervention to improve the physical recovery of the older injured patient.
Primary hypothesis: In comparison to the older injured patients randomized to usual care, those randomized to the TMH intervention will have the following at 6 and 12-month follow-ups:
• Higher physical performance as measured by the short physical performance battery (SPPB);
• Higher scores on the Physical Component Summary (PCS) of the Medical Outcomes Study 36-time short form (SF-36).
Secondary Specific Aim 2: Evaluate the ability of the TMH intervention to improve the psychological recovery of the older injured patient.
Secondary hypothesis 1: In comparison to older injured patients randomized to usual care, those who are randomized to the TMH intervention will have the following at 6 and 12-month follow-ups:
• Lower mood and anxiety symptoms as measured by the Patient Health Questionnaire–9 (PHQ-9) and the Generalized Anxiety Disorder (GAD-7) scale;
• Higher scores on the Mental Component Summary (MCS) of the SF-36.
[Secondary Specific Aim 3: Evaluate the ability of the TMH intervention to reduce health cost and the TMH cost effectiveness relative to usual care of the non-neurologically injured patient.
Secondary hypothesis 2: In comparison to older injured patients randomized to usual care, those who are randomized to the TMH intervention will have the following at 6 and 12-month follow-ups:
• Fewer emergency department visits and hospital readmissions.
• Savings in healthcare utilization in the intervention arm will offset the intervention costs.]
Primary hypothesis: In comparison to the older injured patients randomized to usual care, those randomized to the TMH intervention will have the following at 6 and 12-month follow-ups:
• Higher physical performance as measured by the short physical performance battery (SPPB);
• Higher scores on the Physical Component Summary (PCS) of the Medical Outcomes Study 36-time short form (SF-36).
Secondary Specific Aim 2: Evaluate the ability of the TMH intervention to improve the psychological recovery of the older injured patient.
Secondary hypothesis 1: In comparison to older injured patients randomized to usual care, those who are randomized to the TMH intervention will have the following at 6 and 12-month follow-ups:
• Lower mood and anxiety symptoms as measured by the Patient Health Questionnaire–9 (PHQ-9) and the Generalized Anxiety Disorder (GAD-7) scale;
• Higher scores on the Mental Component Summary (MCS) of the SF-36.
[Secondary Specific Aim 3: Evaluate the ability of the TMH intervention to reduce health cost and the TMH cost effectiveness relative to usual care of the non-neurologically injured patient.
Secondary hypothesis 2: In comparison to older injured patients randomized to usual care, those who are randomized to the TMH intervention will have the following at 6 and 12-month follow-ups:
• Fewer emergency department visits and hospital readmissions.
• Savings in healthcare utilization in the intervention arm will offset the intervention costs.]
Status | Active |
---|---|
Effective start/end date | 4/1/17 → 3/31/21 |
Funding
- Indiana University (IN4688176NW//1R01AG0542493-04)
- National Institute on Aging (IN4688176NW//1R01AG0542493-04)
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