- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01466140
Effects of Writing Down the Request for Help on Patient Satisfaction in General Practices
November 4, 2011 updated by: Nanne Kleefstra
Effects of Writing Down the Request for Help With Regard to Patient Satisfaction in General Practices
The primary objective of this study is to determine whether exploring the request for help more thoroughly improves patient satisfaction in general practice (primary care).
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Patient satisfaction has been an important topic of interest in primary health care during the last decade(s).
Many factors during the consultation influence patient satisfaction.
One of the aspects in a consultation is the request for help; especially in primary care the request for help has been recognised as an important aspect influencing patient satisfaction.
The investigators hypothesized that exploring the request for help more thoroughly would improve patient satisfaction in general practice.
Study Type
Interventional
Enrollment (Actual)
209
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Overijssel
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Zwolle, Overijssel, Netherlands, 8025 AB
- Isala Clinics
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All patients with a new request for help.
Exclusion Criteria:
- Dementia
- Mental disability
- No or little knowledge of the Dutch language
- Illiteracy
- Limited vision
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
NO_INTERVENTION: Control group
Patients in the control group were asked to participate in a patient satisfaction study.
They were asked to fill in a questionnaire with respect to patient satisfaction.
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|
EXPERIMENTAL: Use of request card
Patients in the intervention group were told that the practice was participating in a patient satisfaction study, and they were given an envelope with information about the 'doorknob phenomenon' and a request card.
The envelope for the control group only consisted of information about a patient satisfaction study, without any information on the 'doorknob phenomenon', and without a request card.
Both groups received the same letter with patient information about the study.
|
Patients in the intervention group could write down their request for help on a request card (with a maximum of 2 questions).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient satisfaction measured with the Consultation Satisfaction Questionnaire
Time Frame: 15-30 minutes (after the consultation patients filled in the questionnaire)
|
The primary endpoint is the 'Professional Care' (PC) scale of the 'Consultation Satisfaction Questionnaire' (CSQ).
In a previous study the score on the PC were 88.2 en 80.9 in the intervention and control groups, respectively.
The standard deviations were 11.8 en 16.1.
For our sample size calculation we used an expected standard deviation of 15.
The sample size required to detect a difference of 7 on the PC scale between the intervention and control group, with a power of 90%, and alpha of 5% (two-tailed), and a standard deviation of 15, was 196 patients.
We rounded this number off to 200.
|
15-30 minutes (after the consultation patients filled in the questionnaire)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient satisfaction measured with the Visual Analog Scale
Time Frame: 15-30 minutes (patients filled in the Visual Analog Scale after the consultation)
|
On a scale of 0-10 patients could fill in the Visual Analog Scale with regard to the patient satisfaction during the consultation
|
15-30 minutes (patients filled in the Visual Analog Scale after the consultation)
|
Doctor satisfaction measured with the Visual Analog Scale
Time Frame: 15-30 minutes (general pracitioners filled in the Visual Analog Scale after the consultation)
|
On a scale from 0-10 general practitioners could fill in the Visual Analog Scale with regard to their own satisfaction about the consultation
|
15-30 minutes (general pracitioners filled in the Visual Analog Scale after the consultation)
|
Duration of the consultation
Time Frame: 15-30 minutes (after the consultation the doctor measured the time with a stopwatch)
|
Duration of the consultation was compared between both groups
|
15-30 minutes (after the consultation the doctor measured the time with a stopwatch)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Henk Bilo, Medical Research Centre
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2011
Primary Completion (ACTUAL)
March 1, 2011
Study Completion (ACTUAL)
May 1, 2011
Study Registration Dates
First Submitted
October 21, 2011
First Submitted That Met QC Criteria
November 4, 2011
First Posted (ESTIMATE)
November 6, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
November 6, 2011
Last Update Submitted That Met QC Criteria
November 4, 2011
Last Verified
November 1, 2011
More Information
Terms related to this study
Other Study ID Numbers
- EffectsPS1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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