Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12617001536358
Ethics application status
Approved
Date submitted
28/07/2017
Date registered
6/11/2017
Date last updated
28/09/2022
Date data sharing statement initially provided
28/09/2022
Date results provided
28/09/2022
Type of registration
Retrospectively registered

Titles & IDs
Public title
Effetiveness of an new model of shared telephonic patient referral between primary health care and hospital health care.
Scientific title
Effectiveness of a new model of telephonic patient referral from primary health care to Internal Medicine consultation to reduce the waiting list period.
Secondary ID [1] 292550 0
NONE
Universal Trial Number (UTN)
U1111-1199-9475
Trial acronym
DETELCOM
Linked study record

Health condition
Health condition(s) or problem(s) studied:
INTERNAL MEDICINE DISEASES 304207 0
Condition category
Condition code
Cardiovascular 303544 303544 0 0
Other cardiovascular diseases
Inflammatory and Immune System 303545 303545 0 0
Other inflammatory or immune system disorders
Public Health 303653 303653 0 0
Health service research

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Patients referrals were carreid out via telephone consultation so that the General Practitoners were able to consult directly the Internal Medicine doctors by telephone in order to obtain an early diagnosis. The time to access to the General Practitioner for the first consultation was from 1 to 3 days. During this first telephone consult between the General Practitioner and the Internal Medicine specialist, they both reached an agreement concerning the treatment, and the complementary tests and future check-up were scheduled. The timing for obtaining the results of the complementary tests was 17 days.
Intervention code [1] 298747 0
Diagnosis / Prognosis
Comparator / control treatment
Control groups patients were referrred to Internal Medicine consultation by the traditional way, which involves a waiting list of 51 days and having to be moved several times to the nearest hospital with Internal Medicine consultation (Riotinto Hospital), which is about one hour from the participants´ locations.
Control group
Active

Outcomes
Primary outcome [1] 302912 0
Change in waiting list time (number of days) from primary health care to internal consultation, assessed by review of medical records available at "Diraya" (institutional medical record system)
Timepoint [1] 302912 0
Baseline (first visit to the General Practitioner) and first visit to Internal Medicine Consultation
Secondary outcome [1] 337689 0
Patient´s acceptance of this new model of referral, which was assessed asking them about their reasons to abandon the trial.
Only 9 patients refused to participate in the trial because they preferred the traditional referral way.
Timepoint [1] 337689 0
Baseline (first visit to the General Practitioner consultation)
Secondary outcome [2] 337690 0
Doctors´ acceptance of this new model of referral, which was assessed asking them about their reasons to abandon the trial.
Only 8 doctors refused to participate in the trial because they thought this way would involve more dedication to each patient.
Timepoint [2] 337690 0
Baseline (first visit to General Practitioner consultation)

Eligibility
Key inclusion criteria
Every patient who needed to be referred to Internal Medicine Hospital Consultation according to the Geeral Practitioners´decision.
General Practitioners from the north area of Huelva (Spain) who agreed to participate in the trial.
Minimum age
18 Years
Maximum age
85 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Whenever the General Practitioner considered that a patient would not get significant benefit from the telephone referral.
Patients who refused to participate in the study
General Practitioners who refused to participate in the trial.

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Central randomisation by computer
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Stratified randomisation: General Practitioners were randomised
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
1.- DESCRIPTIVE ANALYSIS
2.- KRUSKALL-WALLIS TEST
3.- MANN-WHITNEY TEST (p= 0.01 CI 99%)
4.-HODGES-LEHMAN TEST FOR INDEPENDENT SAMPLES

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
Actual
1/03/2016
Date of last participant enrolment
Anticipated
Actual
23/12/2016
Date of last data collection
Anticipated
Actual
12/01/2017
Sample size
Target
150
Accrual to date
Final
154
Recruitment outside Australia
Country [1] 9111 0
Spain
State/province [1] 9111 0
SEVILLE

Funding & Sponsors
Funding source category [1] 297126 0
Self funded/Unfunded
Name [1] 297126 0
NOT APPLICABLE
Country [1] 297126 0
Primary sponsor type
Individual
Name
LUIS MIGUEL AZOGIL LÓPEZ
Address
Centro de Salud de Valverde del Camino
Plaza de la Constitución, s/n
21600 - Huelva. Spain
Country
Spain
Secondary sponsor category [1] 296138 0
Individual
Name [1] 296138 0
ESTHER MARÍA MEDRANO SANCHEZ
Address [1] 296138 0
University of Seville. Faculty of Nursing, Physiotherapy and Podiatry.
Calle Avenzoar, 6
41009 SEVILLE
Country [1] 296138 0
Spain
Secondary sponsor category [2] 296139 0
Individual
Name [2] 296139 0
MARÍA DEL VALLE CORONADO VÁZQUEZ
Address [2] 296139 0
Departamento de Sanidad. Gobierno de Aragón
Edificio Vía Universitas
Vía Universitas, 36 - 8ª planta
50071 Zaragoza (Spain)
Country [2] 296139 0
Spain

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 298300 0
Fundación Andaluza Beturia para la Investigación en Salud (F.A.B.I.S.)
Ethics committee address [1] 298300 0
Ethics committee country [1] 298300 0
Spain
Date submitted for ethics approval [1] 298300 0
10/04/2015
Approval date [1] 298300 0
21/09/2015
Ethics approval number [1] 298300 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 76638 0
Mr LUIS MIGUEL AZOGIL LÓPEZ
Address 76638 0
BALTASAR DE ALCAZAR ST, Nº 4, 1ºC
41008 SEVILLE

AFFILIATION: ANDALUSIAN HEALTH CARE PUBLIC SYSTEM (SISTEMA ANDALUZ DE SALUD)
Country 76638 0
Spain
Phone 76638 0
+ 34 646 500 778
Fax 76638 0
+34 954 486 527
Email 76638 0
[email protected]
Contact person for public queries
Name 76639 0
ESTHER MARÍA MEDRANO SANCHEZ
Address 76639 0
DIEGO ANGULO IÑIGUEZ ST. Nº 6, BLOCK 3, 1º C
41018 SEVILLE

AFFILIATION: UNIVERSITY OF SEVILLE
Country 76639 0
Spain
Phone 76639 0
+34 609 076 282
Fax 76639 0
+34 954 486 527
Email 76639 0
[email protected]
Contact person for scientific queries
Name 76640 0
ESTHER MARIA MEDRANO SANCHEZ
Address 76640 0
DIEGO ANGULO IÑIGUEZ ST. Nº 6, BLOCK 3, 1º C
41018 SEVILLE

AFFILIATION: UNIVERSITY OF SEVILLE
Country 76640 0
Spain
Phone 76640 0
+34 609 076 282
Fax 76640 0
+ 34 954 486 527
Email 76640 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
We are not allowed to share individual participant data because of the Spanish Law of personal data protection and digital rights guarantee (https://www.boe.es/eli/es/lo/2018/12/05/3/con).


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseDETELPROG study. Effectiveness of a new model of scheduled telephone referral from primary care to internal medicine. a randomised controlled study.2019https://dx.doi.org/10.3390/jcm8050688
N.B. These documents automatically identified may not have been verified by the study sponsor.