Ignite Creation Date:
2024-05-06 @ 9:24 AM
Last Modification Date:
2024-10-26 @ 12:13 PM
Study NCT ID:
NCT02971150
Status:
COMPLETED
Last Update Posted:
2017-06-01
First Post:
2016-11-17
Brief Title:
Treatment Resistant Depression and Insomnia in Older Veterans
Sponsor:
VA Pittsburgh Healthcare System
Organization:
VA Pittsburgh Healthcare System
Study Overview
Official Title:
Treatment Resistant Depression and Insomnia in Older Veterans A Pilot Study
Status:
COMPLETED
Status Verified Date:
2017-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this pilot study is to obtain information about older Veterans preferences for treatment of depression and insomnia and to pilot test the feasibility and clinical effect of Brief Behavioral Treatment for Insomnia BBTI BBTI for older Veterans living with Treatment Resistant Depression TRD and insomnia
Detailed Description:
Quantitative and qualitative methods will be used to obtain information to aid in developing treatment approaches appropriate for older Veterans with TRD and insomnia Qualitative data will be gathered to better understand Veterans preferences for treatment approaches particularly relating to preference for pharmacotherapy versus augmentation with a behavioral intervention such as BBTI Using a Randomized Controlled Trial RCT design we will test whether augmentation with BBTI will be acceptable to older Veterans and improve treatment response in those whose depression has not improved with antidepressant pharmacotherapy alone and assess for an association between preference and treatment response Our aims and hypotheses are
Aim 1 To characterize the depression insomnia and relevant clinical and neuropsychiatric characteristics of older Veterans with TRD
H1a In Veterans with TRD Antidepressant History Form ATHF scores will have a positive association with Montgomery-Asberg Depression Rating scale MADRS scores
H1b In Veterans with TRD MADRS scores will have a positive association with Insomnia Severity Index ISI scores
Aim 2 Perform qualitative interviews in older Veterans to collect information about their views of their depression and insomnia and attitudes and preferences for treatment of both depression and insomnia
Aim 3 To examine the feasibility of using BBTI to treat Veterans with TRD and insomnia
H3a Use of BBTI will be feasible in older adults with TRD as defined by acceptability and retention
Aim 4 To determine if antidepressant augmentation with BBTI leads to improvement in scores on MADRS and ISI scales in older Veterans receiving BBTI versus those receiving only antidepressant optimization
H4a Augmentation with BBTI will improve both PHQ-9 and ISI scores relative treatment with antidepressant alone
Aim 1 To characterize the depression insomnia and relevant clinical and neuropsychiatric characteristics of older Veterans with TRD
H1a In Veterans with TRD Antidepressant History Form ATHF scores will have a positive association with Montgomery-Asberg Depression Rating scale MADRS scores
H1b In Veterans with TRD MADRS scores will have a positive association with Insomnia Severity Index ISI scores
Aim 2 Perform qualitative interviews in older Veterans to collect information about their views of their depression and insomnia and attitudes and preferences for treatment of both depression and insomnia
Aim 3 To examine the feasibility of using BBTI to treat Veterans with TRD and insomnia
H3a Use of BBTI will be feasible in older adults with TRD as defined by acceptability and retention
Aim 4 To determine if antidepressant augmentation with BBTI leads to improvement in scores on MADRS and ISI scales in older Veterans receiving BBTI versus those receiving only antidepressant optimization
H4a Augmentation with BBTI will improve both PHQ-9 and ISI scores relative treatment with antidepressant alone
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None