ANTLER 75+
Research type
Research Study
Full title
Antidepressants to prevent relapse in depression in older people (ANTLER 75+ Trial) – a double blind randomised controlled trial to evaluate the effectiveness and cost-effectiveness of continuing antidepressants
IRAS ID
1009793
Contact name
Rob Howard
Contact email
Sponsor organisation
University College London
ISRCTN Number
ISRCTN26190474
Research summary
Depression frequently affects older adults with 1 in 7 requiring treatment. General practitioners often prescribe antidepressants. However, it is unclear how long antidepressants should be continued for once symptoms have improved.
Many individuals are eager to discontinue their antidepressants quickly. However, research involving younger participants, and limited data from older adults, indicate that maintaining antidepressants for at least six months post-recovery can help lower the chance of depression recurrence. The ANTLER clinical trial (adults aged 18-74), showed that continuing antidepressants for 12 months after recovery reduced the likelihood of depression returning by half.
Depression in individuals aged 75 and older may respond differently to treatment compared to younger individuals. Risk factors vary, and older adults are more prone to have additional physical illnesses and conditions that may affect blood supply to the brain, which can reduce the effectiveness of antidepressants and heighten side effects.
We will conduct a similar trial to the ANTLER study, targeting individuals aged 75 and older. Participants will have an equal chance of either continuing antidepressants for a year or reducing their dose before switching to a placebo. All medications provided during the trial will be indistinguishable to ensure that both participants and trial staff are blind to the treatment being administered. The primary focus will be to monitor a relapse of depression, if any, throughout the year-long study.
We will also explore the symptoms of antidepressant withdrawal, effects of these medications on anxiety, memory, and concentration, as well as their side effects. Additionally, we will examine the health and social implications, impact of depression on family life, and the economic consequences of either continuing or discontinuing treatment. The findings will assist doctors in making informed decisions on how to balance the potential benefits and riskREC name
South Central - Hampshire B Research Ethics Committee
REC reference
24/SC/0247
Date of REC Opinion
19 Aug 2024
REC opinion
Further Information Favourable Opinion