Multiple Chemical Sensitivities Clinical Trial
Official title:
A Pilot Trial on the Effect of Mindfulness-based Cognitive Therapy Versus "Treatment as Usual" for Individuals With Multiple Chemical Sensitivities
OBJECTIVES
The objective is to evaluate the effect of an 8-week mindfulness-based cognitive therapy
(MBCT) programme on psychological - and somatic symptoms, and illness perceptions in
individuals with self- reported multiple chemical sensitivities.
PARTICIPANTS
Participants will be recruited among respondents to a survey on the consequences of
self-reported symptoms related to inhalation of airborne chemicals conducted by the Danish
Research Centre for Chemical Sensitivities.
DESIGN
The pilot trial is designed as a randomized trial on the effect of MBCT versus treatment as
usual.
INTERVENTION
The MBCT programme includes 2½ hours of group training at the Psychiatric Centre,
Rigshospitalet once a week for 8 weeks. Furthermore participants are encouraged to practice
at home for up to 45 min per day, 6 days a week during the entire course.
OUTCOME MEASURES
Effect of MBCT will be estimated from individual scores on psychometric scales
Status | Completed |
Enrollment | 39 |
Est. completion date | December 2008 |
Est. primary completion date | September 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: 1. Age > 18 years, 2. Currently living in Zealand, 3. Self - reported adjustments of social life and/or occupational conditions due to symptoms related to inhalation of airborne chemicals, 4. Registered at the Danish Research Centre for Chemical Sensitivities because of self-reported symptoms attributed to common chemical scents, 5. Consulted the Al-lergy Clinic, 6. Rigshospitalet between 1990 and 2006 because of self-reported symptoms related to exposures to common environmental agents, 7. Informed consent Exclusion Criteria: 1. Severe depression 2. Psychotic disorders 3. Medical treatment with antianxiety agents and antidepressants 4. Alcohol - or drug abuse 5. Previous participation in a MBCT programme 6. Lack of informed consent |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Denmark | The Danish Research Centre for Chemical Sensitivities | Gentofte |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Gentofte, Copenhagen |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Symptom Checklist- 92 (SCL-92) | Baseline, four - and eight weeks after start of MBCT course, 3 months after ending MBCT course | No | |
Secondary | Perceived Stress Scale (PSS-10) | Baseline, four - and eight weeks after start of MBCT course, three months after ending MBCT course | No | |
Secondary | The subjective health complaints (SHC) inventory | Baseline, four- and eight weeks after start of MBCT course, 3 months after ending MBCT course | No | |
Secondary | The Brief Illness Perception Questionnaire (Brief IPQ) | Baseline, four - and eight weeks after start of MBCT course, three months after ending MBCT course | No |