Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
42 participants
INTERVENTIONAL
2013-04-30
2015-02-28
Brief Summary
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This pilot trial aims to test the systematic identification of eligible patients, to assess the acceptability of the intervention and to estimate potential treatment effects for a larger trial.
It's a randomised pilot study consisting of patients with MUS in primary care. Patients will be randomized to intervention (usual care and additional psychosomatic therapy) or control condition (usual care alone). Patients will be followed for one year.
Participants are patients consulting their GP more than once with MUS and in which the GP presumes that psychosocial distress is an underlying cause.
The intervention is the psychosomatic therapy delivered by a psychosomatic therapist, consists of a combination of information and education, relaxation therapy and mindfulness, cognitive approaches and activating therapy. This multi-component approach is captured into a protocol in which therapists are able to modify the treatment in order to deliver a tailor-made treatment for patients with MUS.
Primary outcome measures are: the number of patients identified and recruited, perceived symptom severity, measured on a Visual Analogue Scale (VAS) and patients' self-rated symptoms of distress, depression, anxiety and somatization (4DSQ: The Four Dimensional Symptom Questionnaire). Other primary outcome measures are the time needed to include the eligible patients, the number of withdrawals in the intervention and control group, compliance in the therapy group and the number of patients who complete the questionnaires.
Secondary outcome measures are: symptoms of hyperventilation (NHL: Nijmegen Hyperventilation List), physical and mental health status and quality of life (SF-36), and level of functioning (MAF: measure of general functioning). Patient satisfaction with the received therapy is rated on a 5-point Likert-type scale. Medical consumption will be measured by the Cost Diary for medical consumption.
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Detailed Description
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Randomisation: Participating patients (n=60) are equally randomised over two groups, the intervention group (usual care and psychosomatic therapy delivered by a psychosomatic therapist) and the control group (usual care of the GP). For the randomisation we used a random number table, whereas a central and blinded allocation procedure was applied.For the randomisation we used a random number table, whereas a central and blinded allocation procedure was applied.
Patients in the intervention group were asked to complete a questionnaire at baseline, at the end of the intervention (+/- 3 months)and at 6 and 12 months. Patients in the control group completed a questionnaire at baseline, at 3 (equals end of intervention), 6 and 12 months.
Statistical analysis The number of patients identified and recruited by the GP as well as the number of eligible patients who declined to enter the trial were analysed using descriptive statistics. Furthermore, at each stage of the study, we recorded the number of trial participants who completed the study.
The effects of the intervention on the primary outcome measures (VAS and 4DSQ) and the secondary outcome measures (NHL, SF-36 and MAF) were estimated using analysis of covariance with baseline value as a covariate. Data analysis was be performed according to the intention-to-treat principle. Medical consumption was measured using the Cost Diary for medical consumption. Patients recorded their absenteeism and healthcare consumption, such as consulting a GP, hospital, paramedic facilities and alternative medicine. Medication intake was recorded at the start and the end of the study. We used standardised Dutch prices (guide cost research 2009), whereas medication costs were calculated according to the Dutch Pharmaco Therapeutic Compass. Costs by absenteeism were calculated according to the Friction Cost method.
Difference in cost of medical consumption between the control and intervention group were estimated using analysis of covariance with baseline value as a covariate.
Difference in baseline characteristics were analysed with the student's t-test for continue variables and the chi-squared test or Fisher's exact test for categorical variables. P-values of \< 0.05 were considered statistical significant.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Psychosomatic therapy
Psychosomatic therapy consists of a combination of information and education delivery, relaxation therapy and mindfulness, cognitive approaches and activating therapy. This multi-component approach is captured into a protocol in which therapists are able to modify the treatment in order to deliver a tailor-made treatment for patients with MUS. Psychosomatic therapy delivered by a psychosomatic therapist.
Psychosomatic therapy
Psychosomatic therapy delivered by a psychosomatic therapist, consists of a combination of information and education delivery, relaxation therapy and mindfulness, cognitive approaches and activating therapy. This multi-component approach is captured into a protocol in which therapists are able to modify the treatment in order to deliver a tailor-made treatment for patients with MUS.
care as usual
usual care of the general practitioner
care as usual
Usual care of the general practitioner
care as usual
usual care of the general practitioner
Interventions
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Psychosomatic therapy
Psychosomatic therapy delivered by a psychosomatic therapist, consists of a combination of information and education delivery, relaxation therapy and mindfulness, cognitive approaches and activating therapy. This multi-component approach is captured into a protocol in which therapists are able to modify the treatment in order to deliver a tailor-made treatment for patients with MUS.
care as usual
usual care of the general practitioner
Eligibility Criteria
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Inclusion Criteria
* stomach-/abdominal pain,
* back/neck/shoulder pain,
* pain in arms/legs/joints,
* headache, chest pain,
* dizziness,
* fainting spells,
* palpitations of the heart,
* shortness of breath,
* nausea/indigestion,
* feeling tired,
* sleeping disorder and psychosocial distress
Exclusion Criteria
* palliative care,
* severe psychiatric disorders,
* long-lasting injury treatment
* patients who are not able to speak, read and write Dutch
18 Years
80 Years
ALL
No
Sponsors
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Radboud University Medical Center
OTHER
Responsible Party
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Tim olde Hartman
Dr T.C. olde Hartman
Principal Investigators
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Tim C. olde Hartman, MD Phd
Role: PRINCIPAL_INVESTIGATOR
Radboud University Medical Center
Locations
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General Practitioner, Douwes Dekker
Albergen, Overijssel, Netherlands
General Practitioner, Hesselink
Borne, Overijssel, Netherlands
General Practitioner,Tuijnenburg
Enschede, Overijssel, Netherlands
General Practitioner, Kleissen
Haaksbergen, Overijssel, Netherlands
General Practitioner, van der Waart
Hengelo, Overijssel, Netherlands
General Practitioner, Van Rijn
Vriezenveen, Overijssel, Netherlands
M. Oijevaar
Borne, , Netherlands
D.J. Jansen
Julianadorp, , Netherlands
Countries
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References
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Wortman MS, Lucassen PL, van Ravesteijn HJ, Bor H, Assendelft PJ, Lucas C, Olde Hartman TC. Brief multimodal psychosomatic therapy in patients with medically unexplained symptoms: feasibility and treatment effects. Fam Pract. 2016 Aug;33(4):346-53. doi: 10.1093/fampra/cmw023. Epub 2016 Apr 13.
Other Identifiers
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2012/365
Identifier Type: -
Identifier Source: org_study_id
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