Effectiveness Brief Information Advanced Directives Primary Care

NCT03302572 | Unknown

• 1 other identifier: 15/101
• Study Type: interventional
• Target: 330
• Locations: 1 country
• Sites: 1

Brief Summary

The knowledge and completion of advanced directives (ADs) by the population is generally low. Primary care could develop a very important role to inform and assist in the preparation of this document because of its accessibility. Objective: To evaluate the effectiveness of an oral brief information and a brochure administered in primary care to improve the proportion of ADs records. Design: Randomized clinical trial. Ambit: 7 offices from a urban health center which serves about 25,000 users older than 18 years. Material and methods It will be administered randomly triptych and oral brief information about the existence of advance directives for people over 18 to attend the appointment of their family doctor for any reason (intervention group). It will be given the possibility of more extensive information if they wish and collaboration will be offered for the advance directive according to patient preferences. The control group will not receive any information. Follow-up: 3 months. Variables will be: number of people interested in ADs, number of ADs made and demographic data (gender, age, education level, race, comorbidities, religion, testament) in both groups. Statistical analysis: multiple linear regression, Poisson and Cox as response analyzed, with the intervention/control group as the main variable adjusting for potential confounders. Bivariate comparison using Student t test or Mann-Whitney test (continuous variables) and chi-square or Fisher's exact test (categorical variables). 165 subjects were required in the control group and 165 in the intervention group. Conclusion: positive results of this study will bring out the brief information managed by family physicians increases the number of ADs thus facilitating the right to autonomy of the patient.

Conditions

Primary Care; Advance Directives; Randomized Controlled Trial

Keywords

primary care; advance directives; randomized controlled trial

Outcome Measures

Primary Outcomes (1)

• Interest in or performance of advance directives

  Proportion of people interested in or performance of Advance Directives in 3 months in the adult population. They will be obtained at the moment that the patient shows interest in the intervention of when they performance the Advance Directives, or if not, by asking by appointment or by telephone within 3 months of their recruitment

  In 3 months

Secondary Outcomes (3)

• Baseline characteristics of those who perform or are interested in Advanced Directives

  In 3 months

• Baseline characteristics of those performing Advanced directives in intervention group

  In 3 months

• Reasons to performance Advanced directives

  In 3 months

Study Arms (2)

Brief information group

EXPERIMENTAL

Patients will be given brief information about the existence of advance directives after resolving the reason for the visit for which they had come. This information will not last more than 3 minutes and will not be repeated on successive visits within the recruitment period. Also, an informative triptych will be given to the patient so that he can read it at home. These leaflets have been made by the regional Department of Health. They will be advised that we can extend the information or help them to do the document in the near future if they want, we will inform that we would wait for the answer 3 months. In case of interest, they can leave their information in the User Service by specifying name, telephone number and reference doctor or ask for an appointment again.

Other: Brief information group

Control group

NO INTERVENTION

Patients who fall into a control group will only be attended to their reason for visiting and will be asked for the necessary data to obtain the independent variables if they do not appear in their history. If the patient in this group wants the information, he will be excluded from the study because he "refuses to participate."

Interventions

Brief information group OTHER

Patients will be given oral brief information about the existence of advance directives after resolving the reason for the visit for which they had come. This information will not last more than 3 minutes and will not be repeated on successive visits within the recruitment period. Also, an informative triptych will be given to the patient so that he can read it at home. These leaflets have been made by the regional Department of Health. They will be advised that we can extend the information or help them to do the document in the near future if they want, we will inform that we would wait for the answer 3 months. In case of interest, they can leave their information in the User Service by specifying name, telephone number and reference doctor or ask for an appointment again.

Brief information group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients older than 18 years old who go to their family doctor by appointment.

You may not qualify if:

• \- Patients with language barrier
• Patients younger than 18 years (advanced directives not provided for by law)
• Patients with altered decision-making ability according to computerized clinical history by coding in health problems or mentioned in a clinical course of computerized medical history : cognitive impairment, dementia, mental retardation diagnosed. Although there are studies on attitudes towards advanced directives of people with early cognitive impairment (Minimental\> 18), it was decided to discard because the intervention should be brief. The cited study also concludes that this type of patients prefer to delegate decisions to the family.
• Patients who come spontaneously to their family doctor.
• Patients who have already been recruited previously in the study. Patients who may visit by appointment only on more than one occasion will only participate once and subsequent visits for recruitment will be excluded. In addition, there will be no reinforcement of the study intervention in these visits.
• Patients who have already formalized the advanced directives.
• Patients who do not wish to participate in the study.

Sponsors & Collaborators

• Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina: lead

Study Sites (1)

Institu Català de la Salut

L'Hospitalet de Llobregat, Barcelona, 08905, Spain

RECRUITING

Study Officials

• Yolanda Rando

  Institut Català de la Salut

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Yolanda Rando

CONTACT

+34616678030; yolanrando@gmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 18, 2017
• First Posted: October 5, 2017
• Study Start: November 3, 2016
• Primary Completion: March 31, 2018
• Study Completion: March 31, 2018
• Last Updated: October 5, 2017

Record last verified: 2017-09

Data Sharing

• IPD Sharing: Will not share

Locations

ES (1)