Mental Healthcare Advance Directive (India)
MENTAL HEALTHCARE ADVANCE DIRECTIVE
Under Section 5 of the Mental Healthcare Act 2017
REGISTRATION REQUIREMENT: This directive must be registered with the District Mental Health Board to have legal force under the MHA 2017. A Medical Practitioner must certify the maker's mental capacity at the time of execution. Two witnesses (not relatives or facility staff) must sign.
I, [Maker Name], born [Maker DOB] (Aadhaar: [Maker Aadhaar]), residing at [Maker Address], being of sound mind and having mental capacity within the meaning of the Mental Healthcare Act 2017, hereby make this Mental Healthcare Advance Directive on [Execution Date].
My mental health diagnosis (if any): [Mental Health Diagnosis]
1. NOMINATED REPRESENTATIVE
1.1 Pursuant to Section 14 of the Mental Healthcare Act 2017, I nominate [Representative Name] ([Representative Relationship]), mobile: [Representative Contact], address: [Representative Address], as my Nominated Representative to make mental healthcare decisions on my behalf during periods when I lack mental capacity.
1.2 My Nominated Representative is authorised to: communicate my preferences to treating clinicians; consent to or refuse treatments on my behalf consistent with this directive; access my mental health records; represent me before the Mental Health Review Board; and ensure this directive is given effect.
2. TREATMENT PREFERENCES
2.1 Treatments I WISH to receive: [Preferred Treatments]
2.2 Treatments I REFUSE: [Refused Treatments]
2.3 Electroconvulsive Therapy (ECT): [ECT Preference]
2.4 Hospitalisation preferences: [Hospitalisation Preferences]
2.5 Emergency contacts: [Emergency Contacts]
2.6 General wishes and values: [General Wishes]
3. OVERRIDE PROVISION
3.1 I acknowledge that under Section 5(5) of the Mental Healthcare Act 2017, the Mental Health Review Board may override this directive in limited circumstances — only if following the directive would be inconsistent with a good clinical response to treatment or would cause risk of immediate harm to myself or others. The Board must record its reasons and notify my Nominated Representative.
3.2 Except in the circumstances described in Section 5(5), this directive shall be binding on all treating mental health establishments.
4. REVOCATION
4.1 I may revoke or modify this directive at any time while I have mental capacity, by executing a written revocation attested in the same manner as this directive and notifying the District Mental Health Board and all persons holding copies.
5. CERTIFICATION AND REGISTRATION
5.1 I confirm that I have mental capacity within the meaning of the Mental Healthcare Act 2017, that I am making this directive voluntarily, and that I understand its nature and effect.
5.2 This directive shall be submitted to the District Mental Health Board for registration. Copies shall be kept by: (a) myself; (b) my Nominated Representative; (c) the mental health establishment where I receive regular treatment; and (d) the District Mental Health Board.
Directive Maker
________________
Signature
Nominated Representative (acceptance)
________________
Signature
Certifying Medical Practitioner
________________
Signature
Witness 1 (non-relative, non-facility staff)
________________
Signature
Witness 2 (non-relative, non-facility staff)
________________
Signature
What Is a Mental Healthcare Advance Directive (India)?
A Mental Healthcare Advance Directive in India establishes the terms governing the arrangement it covers, giving the parties a clear written record to rely on.
Unlike the general Advance Medical Directive framework under the Supreme Court's guidelines in Common Cause (A Registered Society) v. Union of India (2018) 5 SCC 1, which applies to physical illness and end-of-life care, the MHAD is specifically designed for mental health treatment decisions. The MHA 2017 was enacted to implement India's obligations under the UN Convention on the Rights of Persons with Disabilities (UNCRPD), which India ratified in 2007, shifting the legal framework from the custodial model of the repealed Mental Health Act 1987 to a rights-based model.
Section 3 of the MHA 2017 establishes the right of every person with mental illness to make decisions about their own care and treatment. Section 5(1) provides that every person aged 18 years or above may make an advance directive specifying how they wish to be treated during any future period of incapacity, including which treatments they consent to, which they refuse, the person they wish to be their nominated representative, and the manner in which they wish to be cared for. The nominated representative is appointed under Section 14 and has the authority to make treatment decisions when the maker lacks capacity.
The MHAD must be registered with the District Mental Health Board — established under Section 73 of the MHA 2017 — to have legal effect. Treating mental health establishments are legally bound under Section 5(6) to consult and comply with the registered directive when admitting or treating a person who lacks current capacity. A mental health establishment may override an MHAD only where a Medical Board finds, under Section 5(9), that following the directive would be contrary to the best interests of the person.
The Mental Health Review Boards established under Section 68 of the MHA 2017 oversee compliance with the Act's provisions, including the protection of advance directive rights. The National Human Rights Commission and State Human Rights Commissions also have jurisdiction over violations of rights under the MHA 2017. Forms-legal.com provides this Mental Healthcare Advance Directive template to assist individuals in exercising their statutory rights under the Mental Healthcare Act 2017 across all states and union territories of India.
When Do You Need a Mental Healthcare Advance Directive (India)?
You need a Mental Healthcare Advance Directive if you have been diagnosed with a mental illness — such as schizophrenia, bipolar disorder, major depressive disorder, or any other condition that may cause episodic periods of incapacity — and you wish to have your treatment preferences legally documented for those periods.
The India Mental Healthcare Advance Directive (India) document is essential for anyone who has had previous hospital admissions for mental illness and has formed clear views about which treatments work for them and which they wish to avoid. It prevents unwanted treatment and confirms that treatments that have been helpful in the past are continued.
You should also use this directive to appoint a nominated representative — a trusted person who understands your condition and your preferences — to communicate with medical staff during periods when you cannot do so yourself.
Parties in India should prepare a Mental Healthcare Advance Directive (India) proactively rather than waiting for a dispute to arise. Courts interpret agreements based on the written terms rather than oral representations. Under Indian law, the Indian Contract Act 1872 governs contractual obligations, with Section 10 setting essential requirements for valid agreements. The Companies Act 2013 regulates corporate entities through the Registrar of Companies (ROC) and Ministry of Corporate Affairs (MCA). The Industrial Disputes Act 1947 and state labour commissioners govern employment disputes. The Information Technology Act 2000 and IT (Reasonable Security Practices) Rules 2011 protect personal data. The Income Tax Act 1961 and Goods and Services Tax Act 2017 govern tax obligations through the Central Board of Direct Taxes (CBDT) and GST Council. Where the transaction involves regulated activities, prior approval from the relevant authority may be required before execution.
What to Include in Your Mental Healthcare Advance Directive (India)
A valid Mental Healthcare Advance Directive under Section 5 of the Mental Healthcare Act 2017 must include the following elements to meet statutory requirements and confirm legal enforceability.
Maker's identification: Full name, address, Aadhaar number, date of birth, and a statement of the basis for making the directive — whether the maker has been diagnosed with a specific mental illness (such as schizophrenia, bipolar disorder, major depressive disorder, or obsessive-compulsive disorder) or is making the directive in anticipation of possible future illness.
Treatment preferences — consented treatments: A specific list of mental health treatments the maker wishes to receive during periods of incapacity. This may include named medications (with dosage preferences where known), preferred psychotherapy modalities (cognitive behavioural therapy, dialectical behaviour therapy, family therapy), preferred mental health establishments or hospitals, and consent to voluntary admission under specified conditions.
Treatment preferences — refused treatments: An explicit statement of treatments the maker refuses. Under Section 5(4) of the MHA 2017, the maker may refuse any mental health treatment, including electroconvulsive therapy (ECT). The MHA 2017 prohibits unmodified ECT (without anaesthesia) under Section 95, and ECT on minors is prohibited. Where the maker refuses ECT, this refusal must be clearly stated. Physical restraint and seclusion may also be specifically refused.
Nominated representative: Full name, residential address, contact number, email address, Aadhaar number, and relationship to the maker. The scope of the nominated representative's authority under Section 14 of the MHA 2017 should be specified — whether they have authority to consent to specific treatments, to communicate with medical staff, to request review by the Mental Health Review Board under Section 68, and whether the authority is limited or general.
Witness signatures: Two adult witnesses must sign the MHAD, confirming that the maker appeared to be of sound mind at the time of execution, signed voluntarily, and understood the nature of the document. Under the MHA 2017, witnesses must not be relatives of the maker or employees of any mental health establishment where the maker currently receives treatment.
Medical Practitioner certification: A countersignature by a Medical Practitioner registered under the National Medical Commission Act 2020 (or equivalent state medical council registration), certifying that the maker had mental capacity at the time of execution.
Registration details: The District Mental Health Board to which the MHAD will be submitted for registration under Section 5(5) of the MHA 2017; the applicable state rules specifying the registration procedure; and space for the registration number once assigned.
Revocation procedure: An acknowledgment that the maker may revoke or amend the MHAD at any time under Section 5(7) of the MHA 2017, and that revocation must follow the same execution and registration procedure as the original directive.
Confidentiality: Mental health records are subject to strict confidentiality under Section 23 of the MHA 2017 and the IT (Reasonable Security Practices and Procedures and Sensitive Personal Data or Information) Rules 2011 under the Information Technology Act 2000. Forms-legal.com provides this Mental Healthcare Advance Directive template for individuals exercising their statutory rights under the Mental Healthcare Act 2017 across India.
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Reference this free template in an article, syllabus, or research note:
Forms Legal. (2026). Mental Healthcare Advance Directive (India) (India) [Legal document template]. Forms Legal. https://forms-legal.com/india/estate-planning/healthcare-directives/mental-healthcare-advance-directive-india
"Mental Healthcare Advance Directive (India) (India)." Forms Legal, 2026, https://forms-legal.com/india/estate-planning/healthcare-directives/mental-healthcare-advance-directive-india.
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title = {Mental Healthcare Advance Directive (India) (India)},
year = {2026},
howpublished = {\url{https://forms-legal.com/india/estate-planning/healthcare-directives/mental-healthcare-advance-directive-india}},
note = {Free legal document template. Based on Mental Healthcare Act 2017, s.5}
}Frequently Asked Questions
A Mental Healthcare Advance Directive (MHAD) is a statutory document specifically created under Section 5 of the Mental Healthcare Act 2017 (MHA 2017), which came into force on 29 May 2018. The MHAD is a right granted exclusively to persons who have or have previously had a mental illness, enabling them to specify in advance how they wish to be cared for and treated during future periods when their mental illness renders them incapable of making or communicating decisions. The MHA 2017 represents a paradigm shift in Indian mental health law, moving from a paternalistic model (under the repealed Mental Health Act 1987, which focused on detention and involuntary treatment) to a rights-based model grounded in the United Nations Convention on the Rights of Persons with Disabilities (CRPD), which India ratified in 2007. Section 3 of the MHA 2017 creates a right of every person with mental illness to make decisions about their care and treatment, including the right to give or refuse consent. Section 5(1) of the MHA 2017 provides: 'Every person, who is eighteen years of age or above, may, in anticipation of the time when such person may no longer have capacity to make mental health care or treatment decisions, make an advance directive in writing, specifying...
Under Section 5 of the Mental Healthcare Act 2017, a person may use a Mental Healthcare Advance Directive to specify both the treatments they wish to receive and those they wish to refuse during future periods of incapacity due to mental illness. The scope of what can be specified is broad, reflecting the Act's commitment to respecting individual autonomy. Treatments that can be specified in an MHAD include: (a) Medication preferences — the person can specify particular medications that have worked well for them in the past and wish to continue, or medications they have found harmful and wish to avoid. For example, a person with bipolar disorder may specify that they wish to receive lithium but not olanzapine, based on their past experience; (b) Psychotherapy preferences — the type of psychotherapy (CBT, DBT, psychoanalytic therapy) or specific therapists the person wishes to engage; (c) Hospitalisation preferences — the person can specify whether they consent to voluntary admission, their preferred hospital or mental health facility, and conditions under which they would consent to inpatient treatment; (d) Electroconvulsive therapy (ECT) — this is an area of particular significance. The MHA 2017 prohibits ECT without consent in most circumstances.
Registration of a Mental Healthcare Advance Directive (MHAD) under the Mental Healthcare Act 2017 is a statutory requirement that gives the directive legal force and ensures it is accessible to treating physicians when needed. Registration process under the MHA 2017: (1) The MHAD must be in writing and signed or marked by the person making it ('the maker') in the presence of two witnesses. (2) The witnesses must sign and state that the maker appeared to be of sound mind at the time of execution, signed voluntarily, and understood the nature of the document. The witnesses must not be relatives of the maker or employees of any mental health establishment where the maker is currently receiving treatment. (3) The MHAD must be countersigned by a Medical Practitioner (registered under the National Medical Commission Act 2020 or equivalent) to confirm the maker's mental capacity at the time of execution. (4) The executed MHAD is submitted to the District Mental Health Board (or such authority as notified under the applicable state rules) for registration. (5) The Board registers the directive, assigns it a registration number, and maintains it in a register that is accessible to mental health establishments. Storage and access: A copy of the MHAD is retained by the maker; a copy given to the nominated representative; a copy lodged with the mental health establishment where the maker receives regular treatment; and the registered copy maintained by the District Mental Health Board.
The Mental Healthcare Act 2017 represents a comprehensive transformation of mental health rights in India, moving from the custodial approach of the Mental Health Act 1987 to a human rights-based framework aligned with the UN Convention on the Rights of Persons with Disabilities. Key rights under the MHA 2017 include: (1) Right to access mental healthcare (Section 18): every person with mental illness has a right to access mental health care and treatment from government-run or government-funded mental health services. (2) Right to community living (Section 19): persons with mental illness have a right to live in and be part of the community, and cannot be segregated or institutionalised without justification. (3) Right to make treatment decisions (Section 3): includes the right to give informed consent, the right to refuse treatment, and the right to execute an Advance Directive. (4) Right to designate a nominated representative (Section 14): to make decisions during incapacity. (5) Right against cruel, inhuman treatment (Section 20): prohibits seclusion, chained detention, and unmodified ECT. (6) Right to confidentiality (Section 23): medical records and history of persons with mental illness cannot be disclosed without consent. (7) Right to equality and non-discrimination (Section 21): persons with mental illness have the same rights as any other person, including rights under other laws. (8) Right to legal aid (Section 24): persons with mental illness are entitled to free legal aid.
A Mental Healthcare Advance Directive (India) does not legally require a lawyer in India, and individuals and businesses may draft and execute the document independently. The Mental Healthcare Act 2017 does not mandate legal representation for the creation or signing of this type of document. However, seeking independent legal advice from a qualified India lawyer is recommended for transactions involving substantial financial value, complex regulatory requirements, or cross-border elements where multiple legal jurisdictions may apply. A lawyer can verify that the document complies with all applicable statutory requirements, identify potential risks specific to the transaction, and confirm that the terms adequately protect the interests of all parties involved. The Supreme Court of India has jurisdiction over disputes arising from this type of document, and Registrar of Companies (ROC) may impose additional compliance obligations depending on the nature of the underlying transaction. Professional legal review is particularly advisable where the document will be submitted to government agencies or used as evidence in legal proceedings.
This template is provided for informational purposes only and does not constitute legal advice. Laws vary by jurisdiction and change over time. Consult a qualified attorney for advice specific to your situation.Full disclaimer
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