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CHILDREN AS COMPLAINANTS
IN THE HEALTH AND PERSONAL SOCIAL SERVICES IN NORTHERN IRELAND
3 THE METHODOLOGY OF THE
RESEARCH
The resources available for
this permitted a multi-method approach comprising four main
elements noted below, further details on each method follow
later in this section.
1) Analysis of administrative
data held by the Department of Health Social Services and
Public Safety.
2) A survey by telephone
and post of HPSS Trust complaints staff in Northern Ireland
seeking information on how complaints by or about children
and young people are dealt with (the results are reported
in Sections 5 & 6 of this report)
3) A postal survey of potential
child advocacy organisations to establish the availability
of independent advocacy services for children and young
people who may need them (results are reported in Section
8 of this report)
4) Semi-structured telephone
interviews were carried out with lay people involved in
the health and social services complaints in Northern Ireland
(these are reported in Section 7 of this report)
It was not possible within
the confines of the resources made available for the study
to also interview children, young people and/or their parents
who had made complaints although this would have provided
a very important perspective on the issues involved. It
would have been a costly and time consuming piece of research.
| We recommend that such research
should be undertaken as soon as possible by the Department
of Health, Social Services and Public Safety or the
regional NHS R & D Office as it would provide important
baseline information for the new Children's Commissioner
expected to be appointed in 2002. |
Survey of HPSS Trust Complaints
Staff
All 19 Trusts were phoned
by a researcher and asked to post out a copy of their complaints
leaflet(s). All Trusts responded within ten days. Questionnaires
were then sent out on 31st May 2001 to 19 HPSS trusts (see
Annex 1 for a copy of the questionnaire). Persistent and
extensive follow-up calls were required for questionnaires
which were not returned as requested at the end of July.
Phone calls were made to each non-replying organisation
at least once a week, sometimes twice. In five cases organisations
claimed they had not received the questionnaire and repeat
questionnaires were then faxed or emailed to the five Trusts
concerned. By mid- September three Trusts had still not
replied and a third copy of the questionnaire was sent to
them again on 25th September. By mid-October, 17 out of
19 trusts had replied, a response rate of 89%. No questionnaires
were received from Newry and Mourne and Armagh and Dungannon
Trusts. See Table 4.1 for more detail on response rates.
Table 4.1.HPSS Trust Response
Rates
| |
Community |
Acute |
Combined |
Total |
| Number of Trusts contacted/issued
with questionnaires |
6 |
7 |
6 |
19 |
| Number of Trusts responded as at mid
October |
4 |
7 |
5 |
16 |
The Advocacy Survey
Potential and actual advocacy
organisations were identified from a mailing list supplied
by The Children's Law Centre. 91 organisations (voluntary,
public and private, see Annex 4) which might provide advocacy
services for children, were written to and asked to fill
in a short proforma and supply any relevant information
on their organisation. A total of 36 organisations replied
to this first letter giving a 39% response rate but after
a follow-up letter was sent to the remainder on September
25th the response rate was boosted to 49 or 54%.
Key respondent telephone
interview.
Wilson System Complaints
The four Health Boards were
very helpful in supplying names and addresses of independent
panel members involved in the Wilson procedure. All fifty
independent panel members involved in the Wilson Procedure
within the four Boards were written to in August asking
for their agreement to a telephone interview. Fifteen individuals
agreed to be interviewed (a 36% consent rate) although susbsequently
only 12 were actually available for interview (a 24% participation
rate).
Children Order Complaints
Trusts wished to first contact
the individuals involved with their panels, to ask their
permission before passing on their contact details. These
thirty individuals were written to and six agreed to be
interviewed (20% consent rate).
Five Trusts would not or claimed
they could not identify the lay individuals used in their
Children Order complaints system. The fieldwork process
thus revealed a greater degree of secrecy and confusion
surrounding the Children Order complaints system and procedures
compared with the Wilson system predominantly used by and
for adults.
In total 18 interviews were
held with key informants involved in either the Wilson or
the Children Order HPSS complaints systems. These included
lay panel members, panel chairs and Board convenors.
| We recommend that all Trusts should
be required to have readily accessible lists of those
involved in their complaints procedures and should publish
in their Annual Report the identity of lay persons involved
with the Trust's complaints procedure. |
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