Actively Recruiting
Existential Group Treatment for Older Adults (75+) With Psychological Distress in Primary Care
Led by Göteborg University · Updated on 2025-02-28
140
Participants Needed
7
Research Sites
216 weeks
Total Duration
On this page
Sponsors
G
Göteborg University
Lead Sponsor
V
Vastra Gotaland Region
Collaborating Sponsor
AI-Summary
What this Trial Is About
Symptoms of depression and anxiety are common in older adults, and high suicide rates are observed in this age group in Sweden, as in many countries around the globe. Ageing is accompanied by an increased risk of pain, grief, loss, loneliness, cognitive decline and reduced functional ability, all of which may impact on mental health. Despite these facts, older adults are less likely than their younger counterparts to receive care for their mental health problems. Within primary care, many older adults with symptoms of depression and anxiety do not fully meet diagnostic criteria for clinical diagnosis. However, these subthreshold states, often conceptualized as "psychological distress" are associated with emotional suffering, reduced quality of life and compromised function in daily life. Psychological distress, which is mainly treated in primary care, has been shown to increase after the age of 65, and to peak at ages 80-89. This points to a need for effective interventions for older adults in primary care to reduce the risk of developing clinical depression and anxiety disorders. The overall aim of this clinical study is to evaluate, using a randomized control trial design (RCT), an existential psychological group treatment for older adults (75+) with psychological distress in a primary care setting. Research persons randomized to the control arm will receive supportive telephone calls. Specific research aims include: 1. Do older adults show a) decreased psychological distress, b) decreased experiential avoidance, as well as c) improved quality of life after taking part in existential psychological group treatment? Do those randomized to group treatment have significantly better outcomes compared to those randomized to weekly supportive telephone calls? If so, are the positive effects maintained over time? 2. Is experiential avoidance a mediator in the (potential) reduction of psychological distress? 3. Are there any side effects of existential group treatment/supportive telephone calls? 4. Is an existential psychological group treatment for older adults feasible, based on its fidelity? 5. What are older adults' experiences of participating in the existential psychological group treatment/weekly supportive telephone calls?
CONDITIONS
Official Title
Existential Group Treatment for Older Adults (75+) With Psychological Distress in Primary Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be aged 75 or older
- Have increased levels of psychological distress (GHQ-12 score of 3 or higher)
- Be interested in participating in a research project involving group treatment or supportive telephone calls
You will not qualify if you...
- Currently receiving other psychological treatment
- Diagnosed with dementia or MMSE score 25 or below
- Have severe alcohol use disorder, ongoing post-traumatic stress disorder, psychotic or manic episodes, or other mental health problems needing different treatment
- Inadequate knowledge of Swedish
- Acute suicide risk according to diagnostic interview
AI-Screening
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Trial Site Locations
Total: 7 locations
1
Närhälsan Slottsskogen vårdcentral
Gothenburg, Sweden, 41311
Actively Recruiting
2
Närhälsan Majorna Vårdcentral
Gothenburg, Sweden, 41458
Actively Recruiting
3
Närhälsan Högsbo vårdcentral
Gothenburg, Sweden, 41480
Actively Recruiting
4
Vårdcentralen Wästerläkarna
Gothenburg, Sweden, 426 77
Actively Recruiting
5
Capio vårdcentral Orust
Henån, Sweden, 47332
Actively Recruiting
6
Närhälsan Vårgårda vårdcentral
Vårgårda, Sweden, 44731
Not Yet Recruiting
7
Vårdcentralen Kusten Ytterby
Ytterby, Sweden, 44250
Actively Recruiting
Research Team
I
Isak Erling, Psy M
CONTACT
M
Margda Waern, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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