Telephone Support for Seniors with Depression and Anxiety
Evaluation of the PACE/PACENET BHL Clinical Program
Recruiting
Observational Study
Depression
Anxiety
Pain, Chronic
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 65 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 4,000 (estimated)
- Sponsor
- University of Pennsylvania · Other
Who this trial is looking for
This trial is looking for seniors aged 65 and older who are enrolled in the SUSTAIN Clinical Program. Participants will help evaluate the effects of a telephone-based program designed to support mental health over a period of six months.
Are You a Good Fit for This Trial?
You may be able to join if
- I am 65 years old or older.
- I am a male or female.
- I am participating in the SUSTAIN Clinical Program.
- I am willing to provide consent for a six-month follow-up evaluation.
You may not be able to join if
- I do not meet the inclusion criteria.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
About This Trial
The SUpporting Seniors Receiving Treatment And INtervention (SUSTAIN) program is a telephone-based clinical service designed to help identify and manage behavioral health issues among PACE/PACENET enrollees. The purpose of the current project is to a) explore moderators of treatment response among beneficiaries in the SUSTAIN Clinical Program and b) to evaluate the sustained clinical effects of th…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Aged 65 and older, males and females.
2. Participating in the SUSTAIN Clinical Program
3. For the 6 Month Outcome Research Evaluation, in addition to meeting criteria 1 and 2, willing to provide verbal informed consent to participate in the 6 Month Outcome Research Evaluation…
Contacts