Comparing Interventions for Indoor Air -Related Functional Symptoms (TOSI)
Environmental Illness, Functional Symptoms
About this trial
This is an interventional treatment trial for Environmental Illness focused on measuring Indoor Air, Medically unexplained symptoms, Randomized controlled trial, Cognitive-Behavioral Therapy, Applied relaxation
Eligibility Criteria
Inclusion Criteria:
- Self-assessed work ability not more than 7 (on a scale 0-10, compared to lifetime best) (removed, see below)
- Employed minimum three (3) or more years
- Symptoms related to work environment indoor air (non-industrial workplaces)
- Respiratory symptoms related to indoor air
- And symptoms involve more than one other organ system
- Symptoms onset maximum three years before the study
- Symptoms are recurrent
- Symptoms appear more than one (1) environment or continue after repairs environmental exposure(s)
- No single widely acceptable test of organ system function can explain the symptoms (symptoms are medically unexplained)
- Minimum of one sick leave due to indoor air symptoms during the preceding half year
- Fluent Finnish (write/read/speak) (due the interventions)
Exclusion Criteria:
- six (6) months or more sick leave sick leaves due to indoor air symptoms during the preceding two years and currently unable to work
- Planned changes in the work (for example retirement, study free period, pregnancy etc.) during the study
An acute, untreated medical disorder or illnesses:
- Somatic disease that explains the symptoms
- An acute, untreated mental disorder (depression, bipolar disorder, psychotic disorders, obsessive-compulsive disorder, eating disorders, personality disorders)
- Abuse of narcotics or alcohol or (non-prescribed) medicine
- Developmental disorders
- Psychotherapy (current or has ended preceding two years)
- No inform consent
- Other: Patient refusal; not actively participating working life (retired or unemployed)
Based on a steering group´s advice and agreement (10.10.2014), inclusion criteria (Self-assessed work ability not more than 7, on a scale 0-10, compared to lifetime best) was removed. Recruitment continues without this question as an inclusion criteria.
Sites / Locations
- Finnish Institute of Occupational Health (Finland)
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
Cognitive-Behavioral Therapy (CBT)
Applied relaxation group therapy
Information session (psychoeducation)
There will be ten (10) manualized session, fist 90 minutes and nine (9) 45-minute individual sessions conducted at weekly intervals, last two sessions 2 weeks intervals. One booster session will be conducted three months after the treatment. Sessions include psychoeducation about indoor air related symptoms and personal health behavior factors integrated on patients individual symptomatology, cognitive restructuring, behavioral experiments of patients health promoting behavior, imagery rescripting and relapse prevention. Intervention: Behavioral: Psychotherapy (CBT)
There will be seven (7) manualized session, first 120 minutes and six (6) 90-minute group sessions conducted at weekly intervals, last two sessions 2 weeks intervals. One booster session will be conducted three months after treatment. Sessions include information about indoor air related symptoms, behavioral training and experiments focusing on applied relaxation technique and relapse prevention. Intervention: Behavioral: group therapy (ART) NB: The Applied Relaxation group Therapy won´t be carried out due to slow and prolonged recruiting process (A steering group agreement 4/2015 and the Ethics Committee approval 5/2015 for the change of the study plan).
There will be one (1) manualized 90-minute individual session. The session includes information about indoor air related symptoms and factors affecting individual health behavior. Intervention: Information session (psychoeducation)