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Study identifier: NCT04832295 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: Recruiting

Photo-supported Conversations About Well-being

Condition: Stress Disorder  ·  Sponsor: Kronoberg County Council

PhaseNA
Planned participants50
Who can joinAll sexes, 20 Years to 67 Years
Healthy volunteersNoCheck eligibility criteria ↓
WhereVaxjo, Sweden

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

The aim is to to investigate photo-supported conversations about well-being by the intervention Be WellTM in addition to care as usual within primary care, compared to a control group, for patients with stress-related diagnosis. The intention is to examine the outcomes measures regarding exhaustion, balance of activities in everyday life, client satisfaction, depression and anxiety quality of life, sense of coherence and work ability. The study has been approved by the Regional Ethical Review Board. The project has a quasi-experimental design using mixed methods. A total of 70 patients (35 to the intervention group and 35 to the control group) will be included. Inclusion criteria are patients with stress-related disorder in primary care, aged 20-67 years, who are on sick leave or risk being on sick leave. Exclusion criteria are severe somatic disorders, neuropsychiatric diagnosis, psychosis and language or cognitive problems that implies difficulties to answer questionnaires. After informed consent, the intervention group receive, in addition to care as usual, photo-supported conversations about well-being, that is conducted over time for increased training. The intervention involves 12 sessions takes part during 12-15weeks. With cell phones the patients photograph what they relate to well-being in everyday life. The photos are enlarged and used for reflecting conversations with their therapist. Before and after intervention, and 6 months after intervention the patient mee…

This description comes directly from the study's public registry record.

Talk to the study team

Birgitta A Gunnarsson, PhD  ·  +46470589078  ·  birgitta.gunnarsson@kronoberg.se

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * stress related disorder F43.8 (ICD-10) * stress related disorder F43.9 (ICD-10) * on sick leave * risk being on sick leave Exclusion Criteria: * severe somatic disorders * neuropsychiatric diagnosis * psychosis * language problems that implies difficulties to answer questionnaires * cognitive problems that implies difficulties to answer questionnaires

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Kronoberg County CouncilVaxjo, SwedenRecruiting

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Vaxjo

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