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Effectiveness of the Consent Process

Effectiveness of the Consent Process Used for Outpatient Endoscopy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00630136
Enrollment
20
Registered
2008-03-06
Start date
2008-02-29
Completion date
2008-03-31
Last updated
2010-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parental Consent

Brief summary

The purpose of this study is to evaluate the effectiveness of the consent process currently used for outpatient endoscopy procedures at our hospital. Results from this study will be used to assist in making improvements in the way we communicate with parents, thereby enhancing the ability to provide informed consents.

Detailed description

Obtaining informed consent before performing an invasive medical procedure or treatment is a crucial component of patient care. The manner in which the consent process is conducted impacts the doctor/patient relationship, patient safety and patient satisfaction. Many times, patients sign consent forms without reading or understanding them. Although the form has been signed, true informed consent has not been obtained. While there are many variables that impact the ability to truly consent, ineffective communication between the patient and health care providers hampers the process. Evidence shows that improving the consent process by ensuring effective communication between the child's parent and health care team affords substantial benefit. A consent process well done strengthens the parent-provider relationship. It positively impacts risk management. It improves patient safety. It diffuses would-be litigants by helping parents have realistic expectations of care. The consent process should allow and encourage parents to exercise both their right and their responsibility to take an active role in their child's health care.

Interventions

BEHAVIORALinterview

The parent/LAR who has consented to have their child undergo an outpatient endoscopy procedure will be interviewed prior to the procedure being performed.

Sponsors

Children's Mercy Hospital Kansas City
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult parent or legally authorized representative (LAR) of child who has consented to undergo an out-patient endoscopy at CMHC as a diagnostic procedure * Ability to converse in English * Provided implied consent prior to data collection and verbal consent after data collection to participate in this research study

Exclusion criteria

* Any parent/ LAR under the age of 18 years * Time constraint or verbally stating they do not wish to provide study data prior to child undergoing endoscopy * Stating they do not wish to have these data used as study data after completion of the interview

Design outcomes

Primary

MeasureTime frame
determine if the parent/LAR has an understanding of why the endoscopy procedure has been recommended and what it involvesafter obtaining consent for endoscopy but prior to endoscopy procedure
determine if the parent/ LAR has an understanding of the probable benefits and risks associated with endoscopyafter obtaining consent for endoscopy but prior to endoscopy procedure

Secondary

MeasureTime frame
determine if the parent/LAR knows who will be present during the procedureafter obtaining consent for endoscopy but prior to endoscopy procedure
determine if the parent/LAR has an understanding of the importance of the consent processafter obtaining consent for endoscopy but prior to endoscopy procedure

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026