The Lexicon Institute of Technology is committed to the highest standards of ethical conduct in teaching, research, administration, and community engagement. These guidelines ensure that academic and research activities uphold integrity, transparency, accountability, and respect for human dignity.
Faculty, staff, and students must conduct academic and research work honestly, avoiding plagiarism, fabrication, falsification, or misrepresentation.
All individuals must be treated with dignity and fairness, regardless of background, culture, gender, or belief.
Personal, academic, and research-related information must be kept confidential unless disclosure is legally or ethically required.
Members of the Institute must avoid conflicts of interest, maintain professional boundaries, and use institutional resources responsibly.
All research must be guided by the following principles:
The IRB (also known as the Ethics Review Committee) ensures that all research involving human participants, animals, or sensitive data is reviewed for ethical compliance before commencement.
The IRB will include:
Research misconduct includes fabrication, falsification, plagiarism, unethical treatment of participants, or breach of approval conditions. Sanctions may include:
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Title of Research Project |
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________________________________________________________________________________________________________ |
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Principal Investigator (PI) |
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o Name: ______________________________________________________________________________________________ |
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o Position/Department:: ________________________________________________________________________ |
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o Contact (Email/Phone): ______________________________________________________________________ |
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Co-Investigators (if any) |
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________________________________________________________________________________________________________ |
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Proposed Duration |
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From __________________________________________________ To _______________________________________ |
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Funding Source (if applicable) |
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________________________________________________________________________________________________________ |
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Purpose and Objectives of the Study |
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_______________________________________________________________________________________________________________________________________________ |
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Methodology |
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o Research Design: _________________________________________________________________________________ |
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o Data Collection Methods: ________________________________________________________________________ |
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o Instruments/Tools: ______________________________________________________________________ |
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Participants |
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o Target Population: ____________________________________________________________________ |
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o Sample Size: ________________________________________________________________________ |
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o Recruitment Procedures: ______________________________________________________________________ |
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Inclusion/Exclusion Criteria |
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Informed Consent |
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o How will consent be obtained? _____________________________________________________________________ |
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o Attach draft consent form. |
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Risks and Benefits |
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o Describe potential risks to participants: _____________________________________________________________________ |
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o Describe potential benefits: _____________________________________________________________________ |
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Confidentiality Measures |
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o Data storage and protection: _____________________________________________________________________ |
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o Anonymity/identification procedures: _____________________________________________________________________ |
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Special Populations (if applicable) |
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o Does the study involve vulnerable groups (children, the elderly, differently-abled)? ☐ Yes ☐ No |
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o If yes, describe safeguards: _____________________________________________________________________ |
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Plagiarism & Originality Declaration |
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I confirm that this proposal is original, free from plagiarism, and complies with the Institute’s research ethics policy. |
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2. |
Conflict of Interest Declaration |
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☐ None ☐ Yes (explain): __________________________ |
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Investigator’s Signature: |
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________________________________________________________ Date : _____________________________ |
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HOD/Dean Endorsement: |
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________________________________________________________ Date : _____________________________ |
Before submitting your proposal, ensure the following documents are included:
Completed IRB Application Form
Detailed Research Proposal (objectives, methodology, timeline)
Informed Consent Form (sample copy)
Data Collection Instruments (questionnaires, interview guides, etc.)
Risk Assessment Statement (addressing harm/benefits)
Data Management Plan (storage, access, confidentiality)
Recruitment Materials (if applicable)
Endorsement from HoD/Dean
Copy of Funding Approval Letter (if externally funded)