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Comparing Interventions for Indoor Air -Related Functional Symptoms (TOSI)

Primary Purpose

Environmental Illness, Functional Symptoms

Status
Completed
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Cognitive-Behavioral Therapy (CBT)
Applied relaxation group therapy
Information session (psychoeducation)
Sponsored by
Finnish Institute of Occupational Health
About
Eligibility
Locations
Arms
Outcomes
Full info

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

25 Years - 58 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Self-assessed work ability not more than 7 (on a scale 0-10, compared to lifetime best) (removed, see below)
  2. Employed minimum three (3) or more years
  3. Symptoms related to work environment indoor air (non-industrial workplaces)
  4. Respiratory symptoms related to indoor air
  5. And symptoms involve more than one other organ system
  6. Symptoms onset maximum three years before the study
  7. Symptoms are recurrent
  8. Symptoms appear more than one (1) environment or continue after repairs environmental exposure(s)
  9. No single widely acceptable test of organ system function can explain the symptoms (symptoms are medically unexplained)
  10. Minimum of one sick leave due to indoor air symptoms during the preceding half year
  11. Fluent Finnish (write/read/speak) (due the interventions)

Exclusion Criteria:

  1. six (6) months or more sick leave sick leaves due to indoor air symptoms during the preceding two years and currently unable to work
  2. Planned changes in the work (for example retirement, study free period, pregnancy etc.) during the study
  3. An acute, untreated medical disorder or illnesses:

    1. Somatic disease that explains the symptoms
    2. An acute, untreated mental disorder (depression, bipolar disorder, psychotic disorders, obsessive-compulsive disorder, eating disorders, personality disorders)
    3. Abuse of narcotics or alcohol or (non-prescribed) medicine
    4. Developmental disorders
  4. Psychotherapy (current or has ended preceding two years)
  5. No inform consent
  6. 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

Arm Type

Experimental

Experimental

Experimental

Arm Label

Cognitive-Behavioral Therapy (CBT)

Applied relaxation group therapy

Information session (psychoeducation)

Arm Description

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)

Outcomes

Primary Outcome Measures

15D - instrument
The health-related quality of life (HRQoL) instrument (Sintonen, 2001)

Secondary Outcome Measures

• Generalized Anxiety Disorder (GAD-7)
Self-report measure that assesses anxiety symptoms
Insomnia Severity Index (ISI)
Self-report measure that assesses insomnia severity
The Symptom checkList-90 (SCL-90)
Self-report measure that assesses general psychological and somatic symptoms and severity
The Patient Health Questionnaire (PHQ-9)
Self-report measure that assesses depressive symptoms
Visual Analogue Scale (VAS)
Self-report measure that assesses respiratory symptom severity
The Acceptance and Action Questionnaire-2 (AAQ-2)
Self-report measure focuses on experiential avoidance and psychological inflexibility
Illness Worry Scale (IWS)
Self-report measure that focuses on illness worries and attitudes towards illness
Penn State Worry Questionnaire (PSWQ)
Self-report measure that focuses on mourning and continuous worrying toughs
Need for Recovery (NRF)
Self-report measure that focuses on time needed on the recovery after work day
Strategy and Attribution Questionnaire (SAQ)
Self-report measure focuses on personal attribute strategies.
Self-assessed work ability
Self-assessed work ability (on a scale 0-10) (Tuomi & al. 1998)

Full Information

First Posted
February 20, 2014
Last Updated
August 6, 2018
Sponsor
Finnish Institute of Occupational Health
Collaborators
Finnish Work Environment Fund, The Social Insurance Institution of Finland, The Occupational Health Centre of the city of Espoo, Terveystalo healthcare service company (Finland), Mehiläinen Oy healthcare service company (Finland), The Occupational Health Centre of the city of Vantaa, City of Helsinki
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1. Study Identification

Unique Protocol Identification Number
NCT02069002
Brief Title
Comparing Interventions for Indoor Air -Related Functional Symptoms
Acronym
TOSI
Official Title
Psychosocial Interventions for Indoor Air -Related Functional Symptoms - Randomized Controlled Trial (RCT)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
February 2014 (Actual)
Primary Completion Date
July 29, 2018 (Actual)
Study Completion Date
July 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Finnish Institute of Occupational Health
Collaborators
Finnish Work Environment Fund, The Social Insurance Institution of Finland, The Occupational Health Centre of the city of Espoo, Terveystalo healthcare service company (Finland), Mehiläinen Oy healthcare service company (Finland), The Occupational Health Centre of the city of Vantaa, City of Helsinki

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Environmental Illness, Functional Symptoms
Keywords
Indoor Air, Medically unexplained symptoms, Randomized controlled trial, Cognitive-Behavioral Therapy, Applied relaxation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive-Behavioral Therapy (CBT)
Arm Type
Experimental
Arm Description
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)
Arm Title
Applied relaxation group therapy
Arm Type
Experimental
Arm Description
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).
Arm Title
Information session (psychoeducation)
Arm Type
Experimental
Arm Description
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)
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-Behavioral Therapy (CBT)
Intervention Type
Behavioral
Intervention Name(s)
Applied relaxation group therapy
Intervention Type
Behavioral
Intervention Name(s)
Information session (psychoeducation)
Primary Outcome Measure Information:
Title
15D - instrument
Description
The health-related quality of life (HRQoL) instrument (Sintonen, 2001)
Time Frame
baseline, 3, 6 and 12 months from the baseline
Secondary Outcome Measure Information:
Title
• Generalized Anxiety Disorder (GAD-7)
Description
Self-report measure that assesses anxiety symptoms
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
Insomnia Severity Index (ISI)
Description
Self-report measure that assesses insomnia severity
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
The Symptom checkList-90 (SCL-90)
Description
Self-report measure that assesses general psychological and somatic symptoms and severity
Time Frame
baseline, 6 and 12 months from the baseline
Title
The Patient Health Questionnaire (PHQ-9)
Description
Self-report measure that assesses depressive symptoms
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
Visual Analogue Scale (VAS)
Description
Self-report measure that assesses respiratory symptom severity
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
The Acceptance and Action Questionnaire-2 (AAQ-2)
Description
Self-report measure focuses on experiential avoidance and psychological inflexibility
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
Illness Worry Scale (IWS)
Description
Self-report measure that focuses on illness worries and attitudes towards illness
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
Penn State Worry Questionnaire (PSWQ)
Description
Self-report measure that focuses on mourning and continuous worrying toughs
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
Need for Recovery (NRF)
Description
Self-report measure that focuses on time needed on the recovery after work day
Time Frame
baseline, 3, 6 and 12 months from the baseline
Title
Strategy and Attribution Questionnaire (SAQ)
Description
Self-report measure focuses on personal attribute strategies.
Time Frame
baseline, 6 and 12 months from the baseline
Title
Self-assessed work ability
Description
Self-assessed work ability (on a scale 0-10) (Tuomi & al. 1998)
Time Frame
baseline, 3, 6 and 12 months from the baseline
Other Pre-specified Outcome Measures:
Title
Working Alliance Inventory (WAI)
Description
Self-report measure that assesses three key aspects of the therapeutic alliance: (a) agreement on the tasks of therapy, (b) agreement on the goals of therapy and (c) development of an affective bond; for therapists and the patient of the individual cognitive-behavior therapy
Time Frame
after the first, fifth and the last session of the CBT
Title
Sense of coherence Group (SOC-G-20)
Description
For the group therapy patients to evaluate the groups therapeutic alliance.
Time Frame
after the first, fourth and the last session of the grouptherapy
Title
Satisfaction of the treatment
Description
Questionnaire for the intervention groups patients to evaluate the satisfaction of the treatment and its efficacy.
Time Frame
3, 6 and 12 months from the baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
58 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tiina M. Paunio, MD, PhD
Organizational Affiliation
Finnish Institute of Occupational Health and University of Helsinki
Official's Role
Principal Investigator
Facility Information:
Facility Name
Finnish Institute of Occupational Health (Finland)
City
Helsinki
State/Province
Uusimaa
ZIP/Postal Code
00250
Country
Finland

12. IPD Sharing Statement

Citations:
PubMed Identifier
11491191
Citation
Sintonen H. The 15D instrument of health-related quality of life: properties and applications. Ann Med. 2001 Jul;33(5):328-36. doi: 10.3109/07853890109002086.
Results Reference
background
Citation
Tuomi T Ilmarinen J, Jahkola A, Katajarinne l, Tulkki A (1998) Work ability index. Finnish Institute of Occupational Health, Helsinki.
Results Reference
background
PubMed Identifier
10592988
Citation
Tuomisto MT, Lappalainen R, Tuomisto T, Timonen T. [Applied relaxation in psychiatry and behavioral therapy]. Duodecim. 1996;112(11):960-7. No abstract available. Finnish.
Results Reference
background
PubMed Identifier
32078837
Citation
Selinheimo S, Vuokko A, Hublin C, Jarnefelt H, Karvala K, Sainio M, Suojalehto H, Paunio T. Psychosocial treatments for employees with non-specific and persistent physical symptoms associated with indoor air: A randomised controlled trial with a one-year follow-up. J Psychosom Res. 2020 Feb 12;131:109962. doi: 10.1016/j.jpsychores.2020.109962. Online ahead of print.
Results Reference
derived
PubMed Identifier
30935665
Citation
Selinheimo S, Vuokko A, Hublin C, Jarnefelt H, Karvala K, Sainio M, Suojalehto H, Suvisaari J, Paunio T. Health-related quality among life of employees with persistent nonspecific indoor-air-associated health complaints. J Psychosom Res. 2019 Jul;122:112-120. doi: 10.1016/j.jpsychores.2019.03.181. Epub 2019 Mar 25.
Results Reference
derived
PubMed Identifier
27266771
Citation
Selinheimo S, Vuokko A, Sainio M, Karvala K, Suojalehto H, Jarnefelt H, Paunio T. Comparing cognitive-behavioural psychotherapy and psychoeducation for non-specific symptoms associated with indoor air: a randomised control trial protocol. BMJ Open. 2016 Jun 6;6(6):e011003. doi: 10.1136/bmjopen-2015-011003. Erratum In: BMJ Open. 2017 Apr 22;7(4):e011003corr1.
Results Reference
derived
Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
http://bmjopen.bmj.com/content/6/6/e011003.full.pdf+html

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Comparing Interventions for Indoor Air -Related Functional Symptoms

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