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{{org_field_name}}
Registration Number: {{org_field_registration_no}}
Consent to Care and Treatment Policy
1. Purpose
The purpose of this policy is to define how {{org_field_name}} upholds the legal and ethical principles of consent in all aspects of care and support. Our commitment is to ensure that the people we support are fully informed, involved in every decision about their care, and empowered to exercise their right to choose, accept, or refuse care or treatment at any time.
This policy supports our duty to promote autonomy, protect individual rights, and meet the standards of regulatory bodies. It guides our staff in understanding when and how to seek consent, how to support individuals who may have fluctuating or impaired capacity, and how to record and act on consent appropriately.
We are committed to ensuring that no care or treatment is provided without the person’s agreement, unless legally authorised and justified by law.
2. Scope
This policy applies to all staff employed or contracted by {{org_field_name}} who are involved in delivering care or support, including:
- Direct care staff
- Care coordinators and team leaders
- Managers and senior leadership
- Administrative staff who may handle consent-related documentation
- Agency or temporary workers acting on our behalf
It also applies to external professionals and family members who are involved in supporting or representing the people in our care.
The policy relates to all areas of care delivery, including but not limited to:
- Personal care
- Administration of medication
- Accessing or sharing health or social care records
- Supporting with finances or shopping
- Use of equipment or assistive technology
- Care planning and assessments
3. Related Policies
This policy should be read in conjunction with:
- Personal Planning and Outcomes Policy
- Safeguarding Adults and Children Policy
- Data Protection and Confidentiality Policy
- Medication Management Policy
- Risk Assessment and Positive Risk-Taking Policy
- Equality, Diversity and Human Rights Policy
4. Legal and Regulatory Framework
Our approach to consent complies with the following laws and guidance:
- Adults with Incapacity (Scotland) Act 2000
- Human Rights Act 1998
- Data Protection Act 2018 and UK GDPR
- Health and Social Care Standards (2017)
- SSSC Codes of Practice (2024)
- Care Inspectorate guidance on consent, adult support, and human rights
The HSCS clearly sets the expectation that people should:
- Be treated with respect and dignity
- Be fully involved in decisions about their care
- Not receive care they have not agreed to
This policy also reflects the principles of informed consent, including capacity, voluntariness, and understanding.
5. Policy Statement
{{org_field_name}} is committed to ensuring that consent to care and treatment is:
- Obtained in advance, in a manner the person understands
- Given freely, without coercion or undue influence
- Based on adequate and appropriate information
- Revisited and confirmed regularly
- Properly documented in the personal care plan
- Respected at all times, including the right to withdraw consent
We ensure that staff are trained and supported to recognise the legal and ethical importance of consent, to respond appropriately where consent is refused or withdrawn, and to act in the person’s best interest where legal authorisation is in place.
6. How We Manage Consent Efficiently and Responsibly
6.1. Obtaining Informed Consent
At {{org_field_name}}, informed consent is sought before any care or support begins. This involves:
- Explaining what care or support will involve
- Outlining any risks or alternatives
- Confirming that the person understands and agrees
- Ensuring they feel safe, respected, and not pressured
- Asking the person how they wish to give consent (verbally, in writing, with support tools)
We understand that consent is not a one-off event, but an ongoing dialogue. Consent is revisited regularly, particularly during care reviews or when there is a change in the care plan.
If a person refuses care, this is respected and recorded. Staff must never proceed with care against a person’s wishes unless legal authority applies (see section 6.3).
6.2. Supporting People to Give Consent
We ensure that people are supported to give informed consent by:
- Using accessible language and avoiding jargon
- Providing information in formats suited to the individual (e.g., easy read, pictorial, translated materials)
- Taking time to ensure the person understands
- Encouraging the presence of an advocate, family member, or representative if the person chooses
- Using communication aids for people with sensory or cognitive impairments
We train staff to use supported decision-making approaches, which help individuals feel confident in expressing their preferences and understanding their options.
We follow HSCS Standard 2.12: “If I am unable to make my own decisions at any time, the views of those who know my wishes, such as my carer, independent advocate, formal or informal representative, are sought and taken into account.”
6.3. Consent and Capacity
We recognise that not everyone we support will have the same ability to give informed consent, and that capacity can fluctuate over time or vary depending on the decision to be made.
Where there is doubt about an individual’s capacity, the following process is followed:
- Staff carry out an informal assessment of capacity relevant to the specific decision
- Where appropriate, a formal assessment is requested from a qualified health or social care professional
- If the individual lacks capacity and care or treatment is required, the decision is made in accordance with the Adults with Incapacity (Scotland) Act 2000
- Staff check whether there is a valid Power of Attorney, guardianship order, or advance directive in place
- All decisions are clearly recorded in the care plan and reviewed regularly
Staff are trained to work within legal boundaries and seek management support when capacity is in question. They are reminded that lack of capacity does not mean lack of rights, and all actions must reflect the least restrictive option and the person’s known values and preferences.
6.4. Consent to Share Information
Consent is also required to share information with other professionals or family members. At the point of initial assessment, we:
- Explain what information may need to be shared and with whom
- Ask for the person’s consent to share relevant details (e.g., with GPs, social workers, pharmacies)
- Record any limitations to that consent (e.g., “please do not share with my son”)
- Provide assurance about how we protect personal data in accordance with our Data Protection Policy
If a person refuses consent to share information that may impact their safety or wellbeing, we assess whether a duty of care or legal justification overrides that refusal. Such cases are always discussed with a manager and recorded in detail.
6.5. Withdrawing Consent
A person may withdraw their consent at any time, either verbally or in writing. When this happens:
- Staff respect the decision immediately
- The care task or intervention is paused or stopped
- The reason is explored sensitively and without pressure
- The situation is documented clearly
- The Registered Manager is informed
- The care plan is updated accordingly
In some situations, such as the refusal of essential medication or personal care, we may involve the individual’s GP, social worker, or advocate to support the person in making an informed decision, while continuing to respect their autonomy.
6.6. Staff Training and Awareness
All staff at {{org_field_name}} receive comprehensive training in:
- The legal principles of consent and capacity
- How to obtain and record informed consent
- How to support communication and decision-making
- The difference between consent and compliance
- Responding to refusals and capacity concerns
- Documentation and care planning requirements
Consent is discussed in staff supervision and team meetings to ensure good practice is continuously embedded and reviewed.
The SSSC Codes of Practice reinforce that staff must:
- Promote and protect the rights and interests of individuals (Code 1.1)
- Respect people’s rights to make their own decisions (Code 1.3)
- Be honest and trustworthy in their interactions (Code 3.1)
7. Roles and Responsibilities
Registered Manager
Has overall responsibility for ensuring that all care delivered by {{org_field_name}} is based on informed consent. This includes overseeing training, monitoring practice, and supporting staff in complex or high-risk decisions.
Deputy Manager and Team Leaders
Support staff in seeking, recording, and reviewing consent. Ensure that care plans reflect consent appropriately and that concerns about capacity or refusal are escalated and addressed.
Care Staff
Are responsible for gaining consent before every care activity, reporting any issues, and maintaining respectful, person-centred relationships.
People We Support
Have the right to be fully involved in all decisions about their care and to give or withhold consent at any time, with appropriate support.
8. Policy Review
This policy will be reviewed annually or sooner if:
- There is a change in legislation or national guidance
- Internal audits, incidents, or Care Inspectorate feedback suggest improvement
- Staff, people we support, or stakeholders raise issues about its clarity or application
Responsible Person: {{org_field_registered_manager_first_name}}{{org_field_registered_manager_last_name}}
Reviewed on: {{last_update_date}}
Next Review Date: {{next_review_date}}
Copyright © {{current_year}} – {{org_field_name}}. All rights reserved.