Core ethical principle: autonomy and decisional capacity
A
30-year-old pregnant woman who is
fully alert and able to decide for herself is a competent adult. In research ethics, the inability to read is a
communication barrier, not a loss of
decisional capacity. Therefore, the consent must be obtained
from the woman herself, never from a substitute decision-maker such as her husband. The principle of
respect for persons is operationalized through the informed consent process, and it protects the participant’s autonomy
[1][4].
Why option 1 is correct
When a participant cannot read, the consent information is
read aloud in a language she understands, and her comprehension is verified before she agrees. An
impartial witness observes the entire process and attests that the participant understood the information and consented
freely and voluntarily [1][4]. The participant then signs or places a
thumbmark on the consent form. This approach preserves the woman’s autonomy while accommodating her literacy limitation.
Why the other options are incorrect
| Option | Problem |
|---|
| 2. Give the form to take home so a relative can read it | This transfers the consent discussion to an untrained person and does not verify understanding in a controlled, witnessed setting. The researcher remains responsible for ensuring comprehension [1][3]. |
| 3. Ask her husband to read and sign on her behalf | This violates autonomy. A competent adult must consent for herself; a spouse cannot substitute for her decision [1][4]. |
| 4. Record verbal agreement and skip the signed form | Informed consent requires both a process and documentation. The signed form or thumbmark serves as evidence of the process [1][2]. |
Informed consent as a process, not a single event
Informed consent is not merely obtaining a signature. It is a
continuous process in which the researcher explains the nature, procedures, risks, benefits, and treatment schedules of the study in non-technical, understandable language [1][2]. The consent document has two parts: the
Subject Information Sheet and the
Informed Consent Form [1][2]. Both must be approved by an
Institutional Ethics Committee before use
[1].
Special considerations in low-literacy settings
In settings with low literacy levels, ensuring that participants are fully informed before consenting is a recognized challenge
[3]. Researchers must adapt consent tools to the socio-cultural environment and use strategies such as
verbal explanation, witnessed consent, and thumbmarks to maintain ethical standards
[3][4]. The role of the
independent witness becomes especially important in these contexts to confirm that the participant understood and agreed without coercion
[4].
Key point! Illiteracy does not equal incompetence. The participant retains the right to decide for herself; the nurse’s role is to remove the communication barrier, not to bypass her autonomy.
Watch out! Never let a family member sign for a competent adult unless the adult is legally determined to lack decisional capacity.
References (research sources)
- [1]
Informed Consent Process: Foundation of the Researcher-participant Bond.Research articleSil A, Das NK (2017) · DOI: 10.4103/ijd.IJD_272_17
- [2]
Informed Consent in Biomedical Research: Scopes and Challenges.Research articleChatterjee K, Das NK (2021) · DOI: 10.4103/idoj.IDOJ_83_21
- [3]
Exploring informed consent in HIV clinical trials: A case study in Uganda.RCT/clinical trialSsali A, Poland F, Seeley J (2016) · DOI: 10.1016/j.heliyon.2016.e00196
- [4]
The Challenges of Research Informed Consent in Socio-Economically Vulnerable Populations: A Viewpoint From the Democratic Republic of Congo.Research articleKalabuanga M, Ravinetto R, Maketa V, Muhindo Mavoko H, Fungula B, Inocêncio da Luz R (2016) · DOI: 10.1111/dewb.12090