The Western Norway Mental Health Interface Study on Referral Letters

Sponsor
Helse Fonna (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01374035
Collaborator
University of Bergen (Other), KU Leuven (Other)
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Study Details

Study Description

Brief Summary

The main object to this trial is to study the function of referral letters as a mean to coordinate the care process for adult people when referred from Primary Care to Specialised Mental Health Care. The study will explore if and to what degree the quality of these referral letters can be improved, and the potential improvement's impact on defined patient-, professional and organisational related outcomes. According to Medical Research Council guidelines for evaluating complex interventions, a stepwise design with the use of both qualitative and quantitative methods will be used to conduct a controlled intervention study.

Condition or Disease Intervention/Treatment Phase
  • Other: Quality improvement intervention
N/A

Detailed Description

The study is based on a stepwise progression including four steps. Within step one group interview with four mixed groups of health professionals (both Primary and Specialised Care), patient representatives and managers will be conducted. The groups will give input on firstly, what information they think is important to include in the referral letters, and secondly, what impact they think improved referral letters can have for the organisation and care within Specialised Mental Health Care. Within step two a validated check-list to assess the quality of referral letters will be developed. Within step three outcome measures will be developed and tested. Both step two and three will make use of the results from step one in addition to existing literature and testing. Step four is the intervention study where measures from the former steps will be used.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Interface Between Primary Care and Specialist Mental Health Care - the Referral Letters
Actual Study Start Date :
Aug 1, 2010
Actual Primary Completion Date :
Jun 22, 2016
Actual Study Completion Date :
Dec 13, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Participating GPs

GPs working at randomly selected GP centers/offices within the region that are invited to participate and signs a written informed consent to participate. (N=30-40)

Other: Quality improvement intervention
A complex intervention will be implemented within the group of GPs in the intervention group. It includes participation in defining criteria for good referral letters, information about the correlation between information in the referral letters and outcome, introduction to the guideline, and consecutive feedback on own preformance regarding content of referral letter and outcome for the patient.

No Intervention: Control group

GPs working at randomly selected GP centers/office within the region that are not invited to participate, will form the control group. (N=30-40)

Outcome Measures

Primary Outcome Measures

  1. Length of stay [Day of discharge assessed up to six months]

    From date of admission or onset of out-patient treatment until date of discharge (documented in Electronic Patient Record as end of treatment periode), assessed up to six months from admission.

Secondary Outcome Measures

  1. Response time for referral letters in Specialised Mental Health Care [Referral letters will be followed for the duration of the assessment and prioritation process until response letter is sent, an expected avarage of 10 days.]

    Unit of measure: Number of days from receiving a referral letter to the response letter is sent to the patient and the General Practitioner. The response time for all letters recieved in a six month periode before the intervention to improve the quality of referral letters will be compared with the response time after the intervention.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Referral letters send from a GP to Public Specialised Mental Health Care

  • Referrals for elective assessment or treatment

Exclusion Criteria:
  • Referral letters send from other health personnel

  • Referrals for acute care (within 24 hours)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Helse Fonna Local Health Authorities Haugesund Norway 5504

Sponsors and Collaborators

  • Helse Fonna
  • University of Bergen
  • KU Leuven

Investigators

  • Study Chair: Aslak B Aslaksen, MD, PhD, Faculty of Medicine and Dentistery, University of Bergen, Norway
  • Principal Investigator: Kjell Haug, MD, PhD, Faculty of Medicine and Dentistery, University of Bergen, Norway
  • Principal Investigator: Kris Vanhaecht, RN, PhD, KU Leuven

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Miriam Hartveit, PhD-student, Helse Fonna
ClinicalTrials.gov Identifier:
NCT01374035
Other Study ID Numbers:
  • NSD-24340
First Posted:
Jun 15, 2011
Last Update Posted:
Feb 13, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Miriam Hartveit, PhD-student, Helse Fonna
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 13, 2020