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Clinical Improvement and in Quality of Life-Functional Dyspepsia-

Primary Purpose

Psychogenic Dyspepsia

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Psychological support
No intervention
Sponsored by
Hospital Galdakao-Usansolo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Psychogenic Dyspepsia

Eligibility Criteria

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

Inclusion Criteria:

  • to have chronic upper abdominal symptoms consistent with ROME III criteria for functional dyspepsia
  • to have an endoscopy to exclude structural organic causes at the time of the recruitment

Exclusion Criteria:

  • to have any organic pathology that could explain the dyspeptic symptoms
  • to be using non-steroidal anti-inflammatory drugs (NSAIDs)
  • to suffer physical or psychological impairments preventing them from properly completing the questionnaires

Sites / Locations

  • Galdakao-Usansolo Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Psychological support

No psychological support

Arm Description

Ten weekly sessions, which the first 8 were in group and the last 2 were individuals. It consists on a) an informational session; b) Beck's cognitive-behavioural therapy; and c) progressive-muscle relaxation according to Jacobson

Patients of this group only received the conventional medical treatment, not receiving any psychological support

Outcomes

Primary Outcome Measures

Change From Baseline in DYSPEPSIA RELATED HEALTH SCALE (DRHS)
The Dyspepsia Related Health Scale (DRHS) is a self-reported dyspepsia-specific questionnaire that consists of four scales: severity of common symptoms, pain intensity, pain disability, and satisfaction with dyspepsia-related health. The score, for each scale, ranges between 0 and 100, with 0 representing the most severe situation and 100 the least severe. It also yields a global score that ranges from 0 to 100, with higher scores indicating less severe dyspepsia. The adapted and validated Spanish version of this questionnaire is known as QoL-PEI (Quality of Life in relation to Stomach and Intestinal Problems Questionnaire). Its reliability was found to be satisfactory (Cronbach's alpha 0.92). Its factorial analysis confirmed the four scales found by the DRHS but added a global score scale. The convergent validity was moderate (0.54).

Secondary Outcome Measures

Subjective Clinical Improvement
Subjective clinical improvement was measured by a question about how patients feel in regard to the functional dyspepsia ("In relation to functional dyspepsia, how would you rate your health now? a)much better; b) quite a lot better; c) somewhat better; d) about the same; e) somewhat worse; f) quite a lot worse; g) much worse

Full Information

First Posted
February 25, 2013
Last Updated
March 25, 2019
Sponsor
Hospital Galdakao-Usansolo
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1. Study Identification

Unique Protocol Identification Number
NCT01802710
Brief Title
Clinical Improvement and in Quality of Life-Functional Dyspepsia-
Official Title
Influence of the Combined Psychological and Medical Treatment in the Improvement of Symptoms and Quality of Life in Patients With Functional Dyspepsia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
March 2009 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Galdakao-Usansolo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Functional dyspepsia (FD)is defined as the presence of symptoms thought to originate in the gastroduodenal region with no evidence of structural disease that is likely to explain the symptoms. The cause of this condition is unclear, not being a recognized treatment for it. The conventional treatments for those patients are symptom based. Unfortunately, these medications are not very effective. Patients with FD report poorer health status, mental health, and social functioning than patients with structural gastrointestinal pathology. Our aim is to compare a combined intervention (medical plus psychological intervention) versus conventional intervention (medical intervention)in regard to the health related quality of life, symptomatology, anxiety and depression of those patients. The investigators hypothesized that compared with conventional intervention a combined intervention would yield significantly better short (after treatment) and medium term (six months after treatment) improvement of health related quality of life and symptoms.
Detailed Description
Patients were recruited from the digestive services of Galdakao-Usansolo and Basurto hospitals. They were randomly allocated to the control or experimental group. 82 patients were included in the control group and 76 in the experimental group. Regarding the intervention, the treatment of the control group was a conventional (medical) intervention. It was focused on the most bothersome symptom. Prokinetic (for example cinitapride) or antisecretory agent (for example omeprazole) was prescribed in standard dose. Experimental group received the combined intervention (medical plus psychological intervention). The psychological support consisted of ten weekly sessions, which the first 8 were in group and the last 2 were individuals. In those sessions the patients received a) an information session to increase the patients' knowledge of functional dyspepsia; b) a Beck's cognitive-behavioural therapy focused on modifying the influence of some cognitive issues to gastrointestinal symptoms; c) and progressive-muscle relaxation according to Jacobson, with the aim to provide the ability to relax in certain stress situations. This technique was created for reducing anxiety by alternately tensing and relaxing the muscles. All the patients completed all the self questionnaires at baseline (t0), at the end of the treatment (T1) and at six months follow up (T2). The health related quality of life was assessed by the Dyspepsia Related Health Scale (DRHS), and anxiety and depression were assessed by the Hospital Anxiety and Depression Scale (HADS). Finally, the subjective clinical improvement was also considered and it was measured by a question about how they feel in regard to the functional dyspepsia, with five alternatively responses (a) Much better, b) quite a lot better, c) somewhat better, d) about the same, e) somewhat worse, f) quite a lot worse, g) much worse).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychogenic Dyspepsia

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Psychological support
Arm Type
Experimental
Arm Description
Ten weekly sessions, which the first 8 were in group and the last 2 were individuals. It consists on a) an informational session; b) Beck's cognitive-behavioural therapy; and c) progressive-muscle relaxation according to Jacobson
Arm Title
No psychological support
Arm Type
Active Comparator
Arm Description
Patients of this group only received the conventional medical treatment, not receiving any psychological support
Intervention Type
Behavioral
Intervention Name(s)
Psychological support
Intervention Type
Other
Intervention Name(s)
No intervention
Primary Outcome Measure Information:
Title
Change From Baseline in DYSPEPSIA RELATED HEALTH SCALE (DRHS)
Description
The Dyspepsia Related Health Scale (DRHS) is a self-reported dyspepsia-specific questionnaire that consists of four scales: severity of common symptoms, pain intensity, pain disability, and satisfaction with dyspepsia-related health. The score, for each scale, ranges between 0 and 100, with 0 representing the most severe situation and 100 the least severe. It also yields a global score that ranges from 0 to 100, with higher scores indicating less severe dyspepsia. The adapted and validated Spanish version of this questionnaire is known as QoL-PEI (Quality of Life in relation to Stomach and Intestinal Problems Questionnaire). Its reliability was found to be satisfactory (Cronbach's alpha 0.92). Its factorial analysis confirmed the four scales found by the DRHS but added a global score scale. The convergent validity was moderate (0.54).
Time Frame
Participants will be followed at the recruit moment (t0) after treatment (t1) and six months after treatment (t2)
Secondary Outcome Measure Information:
Title
Subjective Clinical Improvement
Description
Subjective clinical improvement was measured by a question about how patients feel in regard to the functional dyspepsia ("In relation to functional dyspepsia, how would you rate your health now? a)much better; b) quite a lot better; c) somewhat better; d) about the same; e) somewhat worse; f) quite a lot worse; g) much worse
Time Frame
Subjective clinical improvement it is measured after treatment (t1) and six months after treatment (t2)
Other Pre-specified Outcome Measures:
Title
Hospital Anxiety and Depression Scale
Description
It is a 14-item measure: 7 items evaluate depression (the HADS-D subscale) and 7 evaluate anxiety (the HADS-A subscale). For each subscale items range from 0 to 21. A subscale score of 0-7 indicates the absence of anxiety or depression; a score of 8-10 indicates a possible case of anxiety or depression; and a score of 11 or higher indicates the presence of anxiety or depression. It has been adapted and validated in a Spanish population
Time Frame
Participants will be followed at the recruit moment (t0) after treatment (t1) and six months after treatment (t2)

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: to have chronic upper abdominal symptoms consistent with ROME III criteria for functional dyspepsia to have an endoscopy to exclude structural organic causes at the time of the recruitment Exclusion Criteria: to have any organic pathology that could explain the dyspeptic symptoms to be using non-steroidal anti-inflammatory drugs (NSAIDs) to suffer physical or psychological impairments preventing them from properly completing the questionnaires
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victor Manuel Orive, Doctor
Organizational Affiliation
Basurto University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jose Luis Cabriada, Doctor
Organizational Affiliation
Hospital Galdakao-Usansolo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Aitor Orive, Doctor
Organizational Affiliation
Hospital Galdakao-Usansolo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Begoña Matellanes, Psychology
Organizational Affiliation
University of Deusto
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maria Josefa Ulloa, Nurse
Organizational Affiliation
Basurto University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jesus Angel Padierna, Doctor
Organizational Affiliation
Hospital Galdakao-Usansolo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Antonio Escobar, Doctor
Organizational Affiliation
Basurto University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Antonio Bernal, Doctor
Organizational Affiliation
Hospital Galdakao-Usansolo
Official's Role
Study Chair
Facility Information:
Facility Name
Galdakao-Usansolo Hospital
City
Usansolo
State/Province
Bizkaia
ZIP/Postal Code
48960
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
25791668
Citation
Orive M, Barrio I, Orive VM, Matellanes B, Padierna JA, Cabriada J, Orive A, Escobar A, Quintana JM. A randomized controlled trial of a 10 week group psychotherapeutic treatment added to standard medical treatment in patients with functional dyspepsia. J Psychosom Res. 2015 Jun;78(6):563-8. doi: 10.1016/j.jpsychores.2015.03.003. Epub 2015 Mar 11.
Results Reference
result

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Clinical Improvement and in Quality of Life-Functional Dyspepsia-

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