Children’s Wellbeing and Schools Bill

Lord Jackson of Peterborough Excerpts

Thursday 22nd May 2025 Lords Chamber

[Lord Addington (LD)]

My Lords, these are probably the sorts of things that we should be doing in Committee. The noble Baroness introduced these amendments very well but I did, I am afraid—having known him for a long time—see the hand of the noble Lord, Lord Lucas, in them. It is definitely his style, as all those who have known him for a long time would say. These are definitely the sorts of questions that we need answered, about the practicality of what is going to happen. All systems will have their flaws, but this is about having the structure to cope with those flaws. Getting that through would be very valuable.

To give fair warning, I will not move my amendment on the NHS number identifier later on.

[Lord Jackson of Peterborough (Con)]

I support Amendment 50, as well as the amendments in the name of the noble Lord, Lord Farmer, who gives his apologies to your Lordships’ Committee, as he is unable to be here to speak to his own amendments. I do so in the spirit of my noble friend Lady Cash, because these are probing amendments by and large, from a position of broad support for the objectives that the Government have laid down in this part of the Bill. Nevertheless, they are amendments that seek clarity in respect of the proposals that the Government are putting forward.

We need more information about the Government’s intention in adding new Section 16LB to the Children Act 2004. Such scrutiny is essential given that it would enable the Government to set in train a process that will be achieved through regulations—secondary legislation —but nevertheless is very far reaching and potentially re-establishes a regime that, as we have heard previously, was abolished in 2010 by the coalition Government for reasons that I will come on to.

It is hard to disagree with the logic that a single unique identifier would prevent children getting lost in systems that are meant to keep them safe, for example, if they are known by different names or their names are not spelled correctly, as happened in the tragic case of Victoria Climbié. I absolutely concur with my noble friend: the name Maria Colwell and other tragic cases hang over someone like me, who served on a social services committee, and many social workers and other professionals over many years. Ensuring that children do not slip through the net or disappear without services knowing where they have gone is paramount, as so many appalling national scandals involving dead or desperately abused children have shown.

It is appropriate that we look at the history and genesis of ContactPoint. It is important to be mindful of the need for qualitative data, not just quantitative data collection; there is a difference. Hence in 2003, in his report about the death of Victoria Climbié, the noble Lord, Lord Laming, recommended the establishment of a new national children’s database for all children under the age of 16. While scrutinising this report six months later, the Health Select Committee in the other place expressed reservations, saying:

“We believe that establishing a national database for children along the lines envisaged by the Laming Report would represent a major practical and technical challenge that should not be underestimated”.


The committee was instinctively open to the concept, likely for the same reasons that many are advocating for it today: if good data can save children’s lives, it of course needs further exploration. The committee went on to say that the implementation difficulties should not be a deterrent and endorsed the recommendation of the noble Lord, Lord Laming, for a feasibility study to explore the value and practicality of setting up a national database for children.

In 2004, as we heard, trailblazer pilots were conducted to assess the feasibility of implementing a children’s information index. Nine local authorities piloted a range of IT applications and a government study of the indexes concluded that implementation was operationally and technically feasible. By 2009, the Children’s Information Sharing Index had been renamed ContactPoint, with the aim of all local authority ContactPoint management teams having access to the database by autumn 2009. In old money, the estimated development and set-up cost of ContactPoint was £224 million and the estimated maintenance cost in 2009-10 was just under £44 million; most of this latter sum was for local staff to operate, maintain and ensure the security of ContactPoint.

Some giving evidence to the Children’s Wellbeing and Schools Bill Committee in the Commons—and arguing strenuously for the SUI—were among those running ContactPoint back then and benefiting from those sizeable contracts. In their defence, they saw this as part of a bigger package and emphasised the need for early intervention in communities and strong relationships with families. The Children’s Charities Coalition said that,

“to really shift the dial we need further investment in early intervention and early help across our communities, and much greater focus on embedding that consistently and universally”.

It also called for further clarification on how the single unique identifier will be effectively applied.

Returning to the ContactPoint database, which was, as I said, abolished by the incoming Government in 2010, it was designed to contain names, ages, addresses and information of all children aged under 18, as well as information about their parents, schools and medical records. Respected organisations such as the Joseph Rowntree Reform Trust quantified the scale and financial cost of data collection, the methods used to maintain and secure the data, and the treatment of critical issues such as consent, as part of a wider study. Its researchers found that children are among “the most at risk” from what they called Britain’s “database state”, with three of the largest databases set up to support and protect children failing to achieve their aims.

--- Later in debate ---

[Baroness Neville-Rolfe (Con)]

My Lords, I very much hope that the NHS number works, so that we can get on with data sharing. When I spoke in an earlier group, I explained the importance of feedback loops in a successful organisation. The amendment moved by the noble Lord, Lord Hampton, is about using the single unique data system to inform research and commissioning. I think he has a point. The precedent of government-supported HDR UK, which I spoke about in the earlier group, is highly relevant as we found a way to anonymise such data on a consistent basis for research purposes. Indeed, the Minister might find HDR UK a useful collaborator in speeding up her excellent work and avoiding Big Brother fears.

We have heard that the single unique identifier will not be used to create a giant database. I am therefore interested in how the Government can gather aggregated data, for example by NHS trust, social service area, education authority, type of family or medical condition. Examination of such group data can reduce future mistakes and costs, target resources and improve efficiency—all the things that I tend to talk about—and make social services and the police more effective. So I would appreciate an answer about how this can be done if we are ruling out a database—by letter if need be, because it obviously goes slightly beyond the scope of the amendment. I am grateful for all the information that has been given today. It has been very reassuring.

[Lord Jackson of Peterborough (Con)]

My Lords, I rise briefly to support the very good amendment moved by the noble Lord, Lord Hampton. If we are spending significant amounts of money on collecting this data and building a database and we have some of the best research facilities in the world, it seems to be sensible when looking at longitudinal studies to utilise that data properly.

My second and more prosaic point is that maybe I am missing something, but it seems to me that subsection (5) and subsection (14) are at variance with each other. They are quite loosely drafted in new Section 16LB. Will the Minister comment on that, because the great thing about the noble Lord’s amendment is that it has pointed out that there seems to be a discrepancy between the two subsections?

[Baroness Finlay of Llandaff (CB)]

My Lords, I shall briefly speak in support of these amendments and of research. We do not need to have a national database established in order to do research because, first, research has to go through research ethics committees, so that is carefully scrutinised. You could take a representative sample of areas and use properly anonymised data. We can do that now. We can anonymise properly rather than using the old-fashioned pseudo-anonymisation, which was not helpful.

But in all these areas, I am afraid, we lack the evidence that we need to make sure that all our services are best targeted. When we are looking at very vulnerable children, we need to know which flags that are currently yellow flags should become red flags and which items do not show a correlation—although there has been an urban myth that they do correlate—so that the index of suspicion is appropriately targeted. To pick up on the point made by my noble friend earlier about having criteria, it is only through good research that we will get good criteria to determine the point at which we trigger an alert that a child is at risk and get that to happen earlier. It may well be that we are missing some important pointers just because they are not in people’s current consciousness, and there is a real danger in reacting to what I would call urban myths.