Testing the Effect of KnowMAP (Knowledge Management for Renal Transplant Recipients). A Randomized Controlled Study

Sponsor
Oslo University Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04296955
Collaborator
Helse Sor-Ost (Other)
200
1
2
67.7
3

Study Details

Study Description

Brief Summary

A randomized controlled study (RCT) aiming to test the effect of a new health literacy intervention for renal transplant recipients, KnowMAP (knowledge management for renal transplant recipients).

Condition or Disease Intervention/Treatment Phase
  • Other: Motivational interview as a new health communication intervention
N/A

Detailed Description

Every year about 250-300 kidney transplantations are performed at Oslo University Hospital in Norway. Considerable improvements have recently emerged within kidney transplantation in relation to survival and quality of life. However, after transplantation, adherence to immunosuppressive drug therapy and other medical advices is crucial for staying healthy, keeping the graft, and retain good quality of life. In case of graft loss the patient has to return to dialysis, representing reduced functioning, fatigue and negative impact on quality of life. Dialysis also leads to higher costs for the society and in many cases a need for re-transplantation. A key challenge to adherence is the ability to gain access to, understand and use health information, defined as health literacy by the WHO. For renal transplant recipients preparedness for handling information and going through transplantation is essential. Hence, supporting the patients becoming reflective and health literate knowledge users is crucial.

Through a RCT this project aims to test the effect of a new health communication intervention, KnowMAP (knowledge management for renal transplant recipients), as compared with standard care in patients undergoing renal transplantation.

KnowMap is a novel intervention designed by clinicians and researchers at Oslo University Hospital (OUS), University of Oslo (UiO) and University of Stavanger (UiS). The intervention is targeting knowledge management skills of patients by using motivational interview (MI) techniques. It represents 4 sessions of individual patient counselling starting the first week after the transplantation.

Study Design

Study Type:
Interventional
Actual Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Interventional study model: Parallel assignment. 2- arm un-blinded RCT design. The arms are: The intervention: 4 individual patient counseling sessions using adapted motivational interviewing techniques in addition to usual care. Usual care: patients undergo standard patient education program for renal transplant recipients at OUS.Interventional study model: Parallel assignment. 2- arm un-blinded RCT design. The arms are:The intervention: 4 individual patient counseling sessions using adapted motivational interviewing techniques in addition to usual care. Usual care: patients undergo standard patient education program for renal transplant recipients at OUS.
Masking:
None (Open Label)
Masking Description:
Block randomization
Primary Purpose:
Supportive Care
Official Title:
Testing the Effect of a New Health Communication Intervention for Renal Transplant Recipients (KnowMAP).
Actual Study Start Date :
Mar 9, 2020
Actual Primary Completion Date :
Jun 15, 2021
Anticipated Study Completion Date :
Oct 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Health communication intervention

Motivational interview as a new health communication intervention (one arm)

Other: Motivational interview as a new health communication intervention
Same as intervention name

No Intervention: Standard care

Standard care

Outcome Measures

Primary Outcome Measures

  1. Health literacy (HL) [24 months post transplantation]

    HL measured by the HLQ (Health Literacy Questionnaire): The HLQ includes 44 items over nine independent scales, each representing a different element of the overall HL construct. Each scale includes 4-6 items. The first five scales comprise items asking the respondents to indicate level of agreement [ranging from strongly disagree to strongly agree (range 1-4)]. The remaining scales (6-9) have domains of self-reported capability (range 1-5: 'cannot do' to 'very easy'). The questionnaire has no total score, as that could potentially mask individual needs in specific HL domains. The HLQ appears robust for its intended purpose of assessing HL in a range of settings and has shown excellent reliability.

  2. Adherence to immunosuppressive medication [24 months post transplantation]

    The instrument BAASIS (The BAsel Adherence to immunoSuppressIve medication Scale) a self reporting adherence questionnaire measuring patients' taking, skipping, timing (>2 hrs from prescribed time) and dose reduction of drugs. The recall period is limited to four weeks. The BAASIS comprises four questions with a 6-point scale for responses ranging from never (0) to every day (5)

Secondary Outcome Measures

  1. Quality of life and cost-effectiveness estimates relevant to this clinical context [24 months post transplantation]

    using EQ-5D-5L, introduced by EuroQoL in 2009. It is a two pages, standardized generic questionnaire.

  2. Knowledge [24 months post transplantation]

    Using a Norwegian developed questionnaire: "The Transplantation Knowledge Questionnaire"

  3. Occations of graft loss [24 months post transplantation]

    Registred in the Norwegian Renal Registry (NNR)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Kidney transplanted patients > 18 years included within few days after kidney transplantation at Oslo University Hospital

  • Able to speak and understand Norwegian

Exclusion Criteria:
  • Not able to speak or understand Norwegian well enough to be able to fill out forms or have a conversation in Norwegian.

  • Kidney transplanted patient <18 years

Contacts and Locations

Locations

Site City State Country Postal Code
1 Oslo University Hospital Oslo Norway 0424

Sponsors and Collaborators

  • Oslo University Hospital
  • Helse Sor-Ost

Investigators

  • Principal Investigator: Andersen, Oslo University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tone Vidnes, PhD student, Oslo University Hospital
ClinicalTrials.gov Identifier:
NCT04296955
Other Study ID Numbers:
  • 29385
First Posted:
Mar 5, 2020
Last Update Posted:
Jun 29, 2021
Last Verified:
Jun 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tone Vidnes, PhD student, Oslo University Hospital

Study Results

No Results Posted as of Jun 29, 2021