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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02565056
Other study ID # 156756
Secondary ID
Status Completed
Phase N/A
First received September 23, 2015
Last updated May 10, 2016
Start date January 2015
Est. completion date April 2016

Study information

Verified date May 2016
Source University of Lincoln
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the feasibility of conducting a trial to evaluate a self-help treatment for depression in people with end-stage renal disease.


Description:

Chronic Kidney Disease (CKD) is a long-term condition in which the function of the kidneys - to filter out waste products from the blood - slowly declines. When renal function becomes sufficiently low it is described as End Stage Renal Disease (ESRD) and renal replacement therapy (RRT) is likely to be needed to prolong life. The most common type of RRT is haemodialysis, in which the patient's blood is filtered through a machine.

It is estimated that depression is experienced by 20-40% of people with ESRD. Depression not only affects the quality of life of individuals with ESRD but is also associated with higher rates of hospitalisation and poorer physical health outcomes.

Acceptance and Commitment Therapy (ACT) has been found to be an effective treatment for depression and has been used successfully as a self-help treatment. However, no study has examined the effectiveness of an ACT self-help treatment for depression in ESRD. This study aims to assess the feasibility of conducting such a study and will look at suitability of recruitment, assessment methods and the acceptability of the self-help treatment, as well as helping to calculate the number of people needed for a definitive study.

Haemodialysis patients receiving dialysis through an NHS renal service will be invited to participate. To participate they will be consenting, over 18 years of age and experiencing depressive symptoms at a clinical level. Those eligible will be randomly assigned into one of two conditionsÍž a control condition receiving treatment as usual (TAU), and an intervention condition receiving TAU alongside an ACT self-help manual with weekly telephone support. The manual will be completed over six weeks. Both groups will be asked to complete questionnaires prior to intervention and 2 and 4 months post-intervention. Participants from each condition will be asked to participate in interviews to explore their experiences of taking part.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- undergoing haemodialysis treatment at one of three identified units

- receiving haemodialysis treatment for more than 6 months

- moderate depression (as indicated by the PHQ-9)

Exclusion Criteria:

- receiving concurrent psychological treatment

- lacking mental capacity to consent due to cognitive impairment

- inadequate reading ability (indicated by inability to complete PHQ-9 screening measure)

- visual or hearing impairment that would prevent completion of the self-help book or engagement in telephone calls

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Other:
Self help book + telephone support
Self-help book based upon principles of Acceptance and Commitment Therapy

Locations

Country Name City State
United Kingdom Shipley Dialysis Unit, Ilkeston Community Hospital Ilkeston Derbyshire
United Kingdom Mike Cassidy Dialysis Unit, Kings Mill Hospital Mansfield Nottinghamshire
United Kingdom Main Dialysis Unit & Centenary Dialysis Unit (same site), City Hospital Nottingham Nottinghamshire

Sponsors (2)

Lead Sponsor Collaborator
University of Lincoln Nottingham University Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Patient Health Questionnaire (PHQ-9) at 2 and 4 months Validated self-report questionnaire assessing symptoms of depression Baseline; 2 months; 4 months No
Secondary Change in EQ-5D-5L at 2 and 4 months Validated self-report questionnaire assessing health-related quality of life Baseline; 2 months; 4 months No
Secondary Change in Acceptance and Action Questionnaire - 2 (AAQ-2) at 2 and 4 months Validated self-report questionnaire assessing psychological flexibility Baseline; 2 months; 4 months No
Secondary Change in Valued Living Questionnaire (VLQ) at 2 and 4 months Validated self-report questionnaire assessing the extent to which individuals live consistently with their identified values Baseline; 2 months; 4 months No
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