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NCT Number: NCT04832295

Photo-supported Conversations About Well-being

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.

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Key information

Conditions

Stress Disorder Mental Disorders Stress Disorders, Traumatic Trauma and Stressor Related Disorders

Age range

20 year–67 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kronoberg County Council

Vaxjo, 35242, Sweden

Location status: Recruiting

Location contact

Birgitta A Gunnarsson, PhD

CONTACT

[email protected]

+46470589078

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

photo-supported conversations

Other

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: Be Well

Care as usual

Other

Medication, psychological treatment

Primary outcomes

  1. 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

  2. Work ability

    Time frame: Up to 9 months after enrollment

    Work ability measured by Worker Role Self-assessment (WRS-18) (Ekbladh et al., 2000) min=15 , max= 90, the higher the better

Secondary outcomes

  1. 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

  2. Client Satisfaction

    Time frame: Up to 9 months after enrollment

    Client Satisfaction measured by the Client Satisfaction Questionnaire (CSQ) (Larsen et al., 1979) min=8, max=32, the higher the better

  3. Depression and anxiety

    Time frame: Up to 9 months after enrollment

    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

  4. Life quality

    Time frame: Up to 9 months after enrollment

    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

  5. Sense of coherence

    Time frame: Up to 9 months after enrollment

    Sense of coherence measured with the Sense of Coherence Scale (SoC) ((Antonovsky, 1987), min=13, max=91, the higher the better

Other outcomes

  1. 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

Study contacts

Contact information is provided by the study sponsor or research team.

Birgitta A Gunnarsson, PhD

CONTACT

[email protected]

+46470589078

Sponsors and collaborators

Lead sponsor

Kronoberg County Council

Other Gov

Collaborators

  • Göteborg University
  • Jonkoping University
  • Linnaeus University
  • Region Jönköping County

Registry information

Official study title

A Study Protocol of the Photo-supported Conversations About Well-being Intervention in People With Stress Related Illness

Important dates

Study start
2020
Primary completion
2024
Study completion
2026
First posted
Apr 5, 2021
Registry last updated
Jun 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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