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Psychosomatic Therapy, Feasibility and Cost Analysis (PsySom)

Primary Purpose

Medically Unexplained Symptoms, Psychosomatic Therapy

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Psychosomatic therapy
care as usual
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Medically Unexplained Symptoms focused on measuring Medically unexplained symptoms, Somatization, Psychosomatic therapy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

patients with medical unexplained symptoms who consulting the general practitioner more than once for one or more of the 12 most common symptoms:

  • 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:

  • patients wich chronic diseases,
  • palliative care,
  • severe psychiatric disorders,
  • long-lasting injury treatment
  • patients who are not able to speak, read and write Dutch

Sites / Locations

  • General Practitioner, Douwes Dekker
  • General Practitioner, Hesselink
  • General Practitioner,Tuijnenburg
  • General Practitioner, Kleissen
  • General Practitioner, van der Waart
  • General Practitioner, Van Rijn
  • M. Oijevaar
  • D.J. Jansen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Psychosomatic therapy

care as usual

Arm Description

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.

Usual care of the general practitioner

Outcomes

Primary Outcome Measures

The number of patients identified and recruited
The number of patients identified and recruited by the GP
The time needed to include the eligible patients
The time needed to include the eligible patients by the GPs
The number of withdrawals in both groups
the number of patients that withdraw from the study in both groups
Perceived symptom severity
Perceived symptoms severity by patients
Patients' self-rated symptoms of distress, depression, anxiety and somatization
Patients' self-rated symptoms of distress, depression, anxiety ansd somatization measured with the Four Dimensional Symptom Questionnaire (4DSQ)

Secondary Outcome Measures

Symptoms of hyperventilation
symptoms of hyperventilation measured by the NHL (Nijmegen Hyperventilation List) according to patients
Physical and mental status and quality of life
Physical and mental health status and quality of life according to patients are measured by the SF-36
Level of functioning
Level of functioning according to patients are measured by the MAF (measure of general functioning)

Full Information

First Posted
August 27, 2013
Last Updated
September 3, 2015
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01935258
Brief Title
Psychosomatic Therapy, Feasibility and Cost Analysis
Acronym
PsySom
Official Title
Psychosomatic Therapy, Feasibility and Cost Analysis, a Pilot Randomised Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Radboud University Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Medically unexplained symptoms (MUS) are a common and important problem in primary care. Patients repeatedly presenting MUS to their general practitioner (GP) suffer from their symptoms, are functionally impaired, and are at risk of unnecessary and possibly harmful tests, referrals and treatment. Evidence indicate that specific interventions for patients with MUS, such as reattribution therapy and cognitive behavioural therapy are of limited help. According to experts in this field a multi-component approach is most helpful for these patients. 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.
Detailed Description
Recruitment and signed informed consent:Participating GPs (n=6) were asked to enrol each consecutive eligible patient and include 10 patients with MUS each. The GPs presented written information and an informed consent form to these patients. Patients had the opportunity to read the information to consider participation before signing the consent form. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Medically Unexplained Symptoms, Psychosomatic Therapy
Keywords
Medically unexplained symptoms, Somatization, Psychosomatic therapy

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Psychosomatic therapy
Arm Type
Experimental
Arm Description
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.
Arm Title
care as usual
Arm Type
Other
Arm Description
Usual care of the general practitioner
Intervention Type
Other
Intervention Name(s)
Psychosomatic therapy
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
care as usual
Intervention Description
usual care of the general practitioner
Primary Outcome Measure Information:
Title
The number of patients identified and recruited
Description
The number of patients identified and recruited by the GP
Time Frame
one year
Title
The time needed to include the eligible patients
Description
The time needed to include the eligible patients by the GPs
Time Frame
one year
Title
The number of withdrawals in both groups
Description
the number of patients that withdraw from the study in both groups
Time Frame
one year
Title
Perceived symptom severity
Description
Perceived symptoms severity by patients
Time Frame
one year
Title
Patients' self-rated symptoms of distress, depression, anxiety and somatization
Description
Patients' self-rated symptoms of distress, depression, anxiety ansd somatization measured with the Four Dimensional Symptom Questionnaire (4DSQ)
Time Frame
one year
Secondary Outcome Measure Information:
Title
Symptoms of hyperventilation
Description
symptoms of hyperventilation measured by the NHL (Nijmegen Hyperventilation List) according to patients
Time Frame
at baseline, at 3, 6 and 12 months
Title
Physical and mental status and quality of life
Description
Physical and mental health status and quality of life according to patients are measured by the SF-36
Time Frame
at baseline, at 3, 6 and 12 months
Title
Level of functioning
Description
Level of functioning according to patients are measured by the MAF (measure of general functioning)
Time Frame
at baseline, at 3, 6 and 12 months
Other Pre-specified Outcome Measures:
Title
Medical consumption
Description
Medical consumption will be measured by the Cost Diary for medical consumption.
Time Frame
at baseline, at 3, 6 and 12 months
Title
Baseline characteristics of the participants
Description
Patient satisfaction with the received therapy is rated on a 5-point Likert-scale
Time Frame
at baseline, at 3, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with medical unexplained symptoms who consulting the general practitioner more than once for one or more of the 12 most common symptoms: 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: patients wich chronic diseases, palliative care, severe psychiatric disorders, long-lasting injury treatment patients who are not able to speak, read and write Dutch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tim C. olde Hartman, MD Phd
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Practitioner, Douwes Dekker
City
Albergen
State/Province
Overijssel
ZIP/Postal Code
7665 AP
Country
Netherlands
Facility Name
General Practitioner, Hesselink
City
Borne
State/Province
Overijssel
ZIP/Postal Code
Borne
Country
Netherlands
Facility Name
General Practitioner,Tuijnenburg
City
Enschede
State/Province
Overijssel
ZIP/Postal Code
7543 EH
Country
Netherlands
Facility Name
General Practitioner, Kleissen
City
Haaksbergen
State/Province
Overijssel
ZIP/Postal Code
7482 AR
Country
Netherlands
Facility Name
General Practitioner, van der Waart
City
Hengelo
State/Province
Overijssel
ZIP/Postal Code
7559 NM
Country
Netherlands
Facility Name
General Practitioner, Van Rijn
City
Vriezenveen
State/Province
Overijssel
ZIP/Postal Code
7672 GD
Country
Netherlands
Facility Name
M. Oijevaar
City
Borne
ZIP/Postal Code
7622DE
Country
Netherlands
Facility Name
D.J. Jansen
City
Julianadorp
ZIP/Postal Code
1787AE
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
27075027
Citation
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.
Results Reference
derived

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Psychosomatic Therapy, Feasibility and Cost Analysis

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