Environmental Illness Clinical Trial
Official title:
Psychosocial Interventions for Indoor Air -Related Functional Symptoms - Randomized Controlled Trial (RCT)
The aim of the current study is to compare the effictiveness of three different psychosocial therapies for treating functional disorders caused by indoor air problems.
Indoor air -related respiratory and other multiple organ symptoms are common in work
environments in Finland. Symptoms effect on well-being and quality of life and may lead to
impaired social and cognitive functioning and decreased work ability. All indoor air -related
conditions are not explained by underlying physical factors and remain medically unexplained.
Functional disorders are conditions where patients complain of multiple medically unexplained
physical symptoms or physical problems don´t correlate with symptom severity. Indoor air
-related symptoms and functional disorders are strongly associated to each other but there
are no well-established diagnostic criteria for the condition . So far, there is no available
treatment program to the indoor air -related symptoms to offer in primary or occupational
health care services in Finland.
In randomized controlled trials, cognitive behavioral treatment has shown to be effective for
patients suffering from functional disorders. In addition, a relaxation technique entitled as
applied relaxation (Tuomisto & al, 1996) have shown to been shown to been effective to treat
different kind of functional problems.
There are no published trials on treatment for individuals of indoor air related
symptomatology. The present study is designed as a pragmatic trial to investigate the effect
of three different treatment programs as compared to treatment as usual (TAU) for indoor air-
related problems in order to improve the (1) work capacity and (2) well-being. A secondary
aim of the study is to identify psychological factors affecting the patients' response to the
treatment.
The patients are recruited from occupational health care services to establish and to
evaluate the efficacy and usability of the treatment procedures. Participants will first
undergo baseline assessment including medical examination of the respiratory symptoms. Then
they are randomized to one of the study groups: TAU or one of the intervention groups. All
study patients receive TAU at occupational health care services for their medical problems
during the study. Patients randomized to the study groups receive also the intervention with
TAU.
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Status | Clinical Trial | Phase | |
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Completed |
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N/A |