Clinical Trials Directory

Trials / Completed

CompletedNCT02567513

Cost-Effectiveness of Weight Loss Prevention in Nursing Homes: A Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
154 (actual)
Sponsor
Vanderbilt University · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Accepted

Summary

Low oral food and fluid intake and unintentional weight loss are common problems among long-stay nursing home (NH) residents and are associated with adverse, costly clinical outcomes. This study will use a controlled, intervention design to determine the cost-effectiveness of oral liquid nutrition supplements with an alternative nutrition intervention that offers NH residents a choice between supplements and other foods and fluids (i.e., snacks) between meals in a group of 200 residents across 4 NH sites. Residents with an order for supplementation will be included in this study and randomized into one of three groups: (1) usual care control; (2) oral liquid nutrition supplementation intervention; or (3) choice intervention. The usual care control group will continue to receive standard NH care for supplement or snack delivery. Research staff will provide the same supplements used by the NH (group two) or a choice between supplements and other foods and fluids (group three) twice daily, five days per week, for 24 weeks and document the daily costs of intervention implementation when also providing a prompting protocol known to improve intake and enhance independence in eating. Based on extensive preliminary data, it is anticipated that both groups two and three will require significantly more staff time than usual care (group one). Thus, the labor costs of these interventions will be documented and compared to effectiveness measures. Effectiveness measures include the following resident outcomes: improvements in total daily caloric intake, weight, nutrition and hydration status and quality of life. These outcomes will be independently monitored for all three groups across 24-weeks by trained research staff using standardized, validated protocols.

Conditions

Interventions

TypeNameDescription
BEHAVIORALSupplement InterventionSupplements given twice/day, 5 days/week, for 24 weeks by research staff.
BEHAVIORALSnack InterventionSnacks given twice/day, 5 days/week for 24 weeks by research staff.

Timeline

Start date
2009-10-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2015-10-05
Last updated
2015-10-06

Source: ClinicalTrials.gov record NCT02567513. Inclusion in this directory is not an endorsement.