- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04832295
Photo-supported Conversations About Well-being
A Study Protocol of the Photo-supported Conversations About Well-being Intervention in People with Stress Related Illness
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 meets a project assistant and respond questionnaires as well as qualitative interviews. The control group has the same measure points. Outcome measures are compared with a control group who receive care as usual in primary care. Data will be collected by questionnaires for exhaustion, balance of activities in everyday life, client satisfaction, depression and anxiety, quality of life, sense of coherence and work ability. Qualitative data from interviews about life situation and treatment experiences will also be analyzed. An additional aim is to investigate how therapists experience performing a health promoting intervention, collected from qualitative interviews.
The project is involving the Kronoberg County Council and Jönköping County Council. Gatekeepers will recruit patients and occupational therapists will perform the intervention. The research team comprise of researchers from Kronoberg County Council, Linnaeus University, Jönköping University and University of Gothenburg.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The project has the following research questions:
- How are the participants' work ability, health and well-being affected by the photo-supported intervention?
- Primary outcome is self-rated symptoms of exhaustion.
- Secondary outcomes are self-rated balance of activities in everyday life, client satisfaction, depression and anxiety, quality of life, sense of coherence and work ability.
The interviews deals about:
- How do the participants perceive their life situation, within as well as beyond paid work, before and after the intervention?
- How do the participants perceive their participation photo-supported conversations about well-being intervention (Be Well)?
- How do the therapists perceive the delivery of the intervention "Be Well"?
Non-parametric statistics will be used for analyzing quantitative data. Thematic, phenomenological, qualitative content analyses and semiotic methods will be used for qualitative data.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Birgitta A Gunnarsson, PhD
- Phone Number: +46470589078
- Email: birgitta.gunnarsson@kronoberg.se
Study Locations
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-
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Växjö, Sweden, 35242
- Recruiting
- Kronoberg County Council
-
Contact:
- Birgitta A Gunnarsson, PhD
- Phone Number: +46470589078
- Email: birgitta.gunnarsson@kronoberg.se
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Intervention
Photo-supported conversations about well-being, in addition to care as usual
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Sessions 1-4: Before each of the sessions, the client photographs that which is related to their well-being and send these to the therapist before the session. The therapist enlarges each of the photographs into the size of A4. The conversation departures from the photographs and the client is encouraged to talk about each of them and they ways it relates to their well-being. Potential strategies for everyday life are discussed. Session 5-10: short virtual meetings of approximately 15-20 minutes with the aim to follow the client, confirm their process and support them towards increased well-being. Session 11: reflecting upon all their previous photographs. Session 12: reflecting future everyday life upon their photographs.
Other Names:
Medication, psychological treatment
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Active Comparator: Control
Care as usual
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Medication, psychological treatment
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exhaustion
Time Frame: Up to 9 months after enrollment
|
Symptoms of exhaustion measured by Karolinska Exhaustion Disorder Scale (KEDS) (Besèr et al., 2014) min=0 , max=54 , the higher the worse
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Up to 9 months after enrollment
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Work ability
Time Frame: Up to 9 months after enrollment
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Work ability measured by Worker Role Self-assessment (WRS-18) (Ekbladh et al., 2000) min=15 , max= 90, the higher the better
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Up to 9 months after enrollment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance of activities in everyday life
Time Frame: Change from baseline to after treatment, and 6 months
|
Balance of activities in everyday life measured by the Occupational Balance questionnaire (OBQ11) (Håkansson et al., 2020) min=0 , max=33, the higher the better
|
Change from baseline to after treatment, and 6 months
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Client Satisfaction
Time Frame: Up to 9 months after enrollment
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Client Satisfaction measured by the Client Satisfaction Questionnaire (CSQ) (Larsen et al., 1979) min=8, max=32, the higher the better
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Up to 9 months after enrollment
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Depression and anxiety
Time Frame: Up to 9 months after enrollment
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Symptoms of Depression and anxiety measured by the Hospital Anxiety and Depression Scale (HADS) (Zigmond & Snaith, 1983), min=0, max=42, the higher the worse
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Up to 9 months after enrollment
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Life quality
Time Frame: Up to 9 months after enrollment
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Quality of life measured with the Manchester Short Assessment of quality of life (MANSA) (Priebe et al., 1999), min=12, max=84, the higher the better
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Up to 9 months after enrollment
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Sense of coherence
Time Frame: Up to 9 months after enrollment
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Sense of coherence measured with the Sense of Coherence Scale (SoC) ((Antonovsky, 1987), min=13, max=91, the higher the better
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Up to 9 months after enrollment
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Interview
Time Frame: Up to 9 months after enrollment
|
situation in everyday life, and what causes stress at home and at work, and what contributes to well-being despite living with stress
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Up to 9 months after enrollment
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Birgitta A Gunnarsson, PhD, Kronoberg County Council
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FORSS-847271
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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