RCT of the Clinical and Cost Effectiveness of Cognitive Behaviour Therapy (CBT) Delivered Remotely Versus Treatment as Usual in Adolescents and Young Adults With Depression Who Repeatedly Self-harm (eDASH)
Primary Purpose
Depression and Self-Harm
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Problem solving cognitive behaviour therapy (PS CBT)
Sponsored by
About this trial
This is an interventional treatment trial for Depression and Self-Harm
Eligibility Criteria
Inclusion Criteria:
- >2 self-harm episodes.
- With high levels of unipolar depressive symptoms (BDI-2 score of 17 or more).
- Sufficient understanding of English (spoken and written).
- Ability to give informed consent
Exclusion Criteria:
- Clinical judgement of high level of suicide risk, other risk to self or others requiring other urgent approaches e.g. admission to mental health unit.
- Other severe mental illness e.g. psychosis, bipolar disorder, substance use disorder or organic mental disorder e.g. secondary to head injury as the primary mental health problem as determined by a structured psychiatric interview (SCID).
- Currently receiving structured psychological therapy
Sites / Locations
- Derbyshire Healthcare NHS Foundation Trust
- Derbyshire Hoispitals NHS Foundation Trust
- Chesterfield Royal Hospital NHS Foundation Trust
- Nottinghamshire Healthcare NHS foundation Trust.
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
PS CBT
Treatment as Usual
Arm Description
Problem solving cognitive behaviour therapy (PS CBT) will be delivered remotely by means of telephone or video calling by a cognitive behaviour therapist in addition to their usual care. The duration of the intervention will be 10 sessions. Research measures will be completed at baseline, 3,6,9 and 12 months
Participants will not receive any CBT therapy in addition to their usual care. Research measures will be completed at baseline,3,6,9 and 12 months.
Outcomes
Primary Outcome Measures
Beck Depression Inventory (V2)
The difference of change in self-rated depression as measured by Beck depression inventory (version 2) from baseline to 6 months, between the control and intervention group.
Secondary Outcome Measures
Beck Depression Inventory (V2)
Time to Self-Harm
Time to self-harm, assessed through a self-report measure and verified through medical records where possible
Patient Health Questionnaire 9
Depressive symptoms on the PHQ-9 (Kroenke et al, 2001)
Beck hopelessness scale
Hopelessness measured on the Beck hopelessness scale (Beck, 1988)
Columbia Suicide Severity Rating Scale
Suicidality measured on the Columbia Suicide Severity Rating Scale (CSSRS; Posner et al, 2011).
Social functioning
Social functioning measured using the work and social adjustment scale (WSAS; Mundt et al, 2002).
Quality of life
Quality of life measured using EQ-5D (EuroQol Group, 1990).
Cost Effectiveness
A modified version of the Client Service Receipt Inventory (CSRI; Beecham & Knapp, 2001): to measure costs, service utilisation, income and related matters to analyse cost effectiveness.
Qualitative Interviews
Explore reasons why individuals may or may not engage with the study and the PS CBT intervention
Full Information
NCT ID
NCT02377011
First Posted
February 25, 2015
Last Updated
January 16, 2018
Sponsor
University of Nottingham
1. Study Identification
Unique Protocol Identification Number
NCT02377011
Brief Title
RCT of the Clinical and Cost Effectiveness of Cognitive Behaviour Therapy (CBT) Delivered Remotely Versus Treatment as Usual in Adolescents and Young Adults With Depression Who Repeatedly Self-harm
Acronym
eDASH
Official Title
Randomised Controlled Trial of the Clinical and Cost Effectiveness of NICE Recommended Problem Solving Cognitive Behaviour Therapy (PS CBT) Delivered Remotely Versus Treatment as Usual in Adolescents and Young Adults With Depression Who Repeatedly Self-harm
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nottingham
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A randomized controlled trial to test the whether remote delivery of cognitive based therapy (CBT) is clinically and cost effective when compared to treatment as usual in adolescents and young adults with depression who self-harm.
Detailed Description
Self harm is one of the five leading causes of admission to acute hospital with rates increasing by nearly 50% from 2003-2009 (South West Public Health Observatory, 2012). Re-admission within 30 days is frequent. People who repeatedly self harm are at high risk for suicide and and as a result suicide, self-harm and crisis are priorities for CCGs and HWBs in the East Midlands.
The NICE Clinical Guideline 133 on longer-term treatment of self-harm recommends between 3 to 12 sessions of psychological treatment involving problem solving and alternative coping. Presently however, the biggest at risk group for self-harm and suicide is not offered any psychological treatment.
Studies have shown that mobile phones are a highly acceptable method of engaging adolescents with depression in psychological treatments such as CBT (Whittaker et al 2012). Furthermore a systematic review has show that treatment delivery via remote technology is just as effective as face-to-face in people with anxiety or depression (Bee et al, 2008).
The study therefore has the following aims and objectives:
To optimise and determine the acceptability and feasibility of engaging and retaining patients with depression who repeatedly self-harm in a remotely delivered (through video calling/telephone) CBT intervention over 10 sessions.
To outline the barriers and drivers to delivering both the study and the remotely delivered PS CBT intervention and how barriers to the interventions are addressed through a network of practice or other means.
If the recruitment and retention into the study and the remotely delivered PS therapy are feasible and acceptable, then we will determine the clinical effectiveness and cost effectiveness of the intervention versus treatment as usual.
If the intervention (pilot study) proves to be clinically effective and cost effective then the barriers and drivers to implementation in all counties in the East Midlands will be explored using a network of practice linking with NHS organisations, strategic clinical networks, and the AHSN (see qualitative analysis of barriers and drivers to the implementation of the intervention below).
The main hypothesis of this study is:
Adolescents and young adults who receive problem solving cognitive behaviour therapy (plus treatment as usual) will report greater reduction in their depressive symptoms (as measured using Beck depression inventory 2) from baseline to 6 months in comparison to those receiving treatment as usual.
Secondary objectives will be to observe a change over 12 months on measures of depression, hopelessness and suicidality.
Study configuration:
This study will compare two groups: participants will be randomly assigned to the TAU group (control group) or the remotely delivered PS CBT (and TAU) group (intervention group).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression and Self-Harm
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PS CBT
Arm Type
Experimental
Arm Description
Problem solving cognitive behaviour therapy (PS CBT) will be delivered remotely by means of telephone or video calling by a cognitive behaviour therapist in addition to their usual care.
The duration of the intervention will be 10 sessions. Research measures will be completed at baseline, 3,6,9 and 12 months
Arm Title
Treatment as Usual
Arm Type
No Intervention
Arm Description
Participants will not receive any CBT therapy in addition to their usual care. Research measures will be completed at baseline,3,6,9 and 12 months.
Intervention Type
Behavioral
Intervention Name(s)
Problem solving cognitive behaviour therapy (PS CBT)
Primary Outcome Measure Information:
Title
Beck Depression Inventory (V2)
Description
The difference of change in self-rated depression as measured by Beck depression inventory (version 2) from baseline to 6 months, between the control and intervention group.
Time Frame
Baseline to 6 months
Secondary Outcome Measure Information:
Title
Beck Depression Inventory (V2)
Time Frame
Baseline to 12 months
Title
Time to Self-Harm
Description
Time to self-harm, assessed through a self-report measure and verified through medical records where possible
Time Frame
Baseline to 12 months
Title
Patient Health Questionnaire 9
Description
Depressive symptoms on the PHQ-9 (Kroenke et al, 2001)
Time Frame
Baseline to 12 months
Title
Beck hopelessness scale
Description
Hopelessness measured on the Beck hopelessness scale (Beck, 1988)
Time Frame
Baseline to 12 months
Title
Columbia Suicide Severity Rating Scale
Description
Suicidality measured on the Columbia Suicide Severity Rating Scale (CSSRS; Posner et al, 2011).
Time Frame
Baseline to 12 months
Title
Social functioning
Description
Social functioning measured using the work and social adjustment scale (WSAS; Mundt et al, 2002).
Time Frame
Baseline to 12 months
Title
Quality of life
Description
Quality of life measured using EQ-5D (EuroQol Group, 1990).
Time Frame
Baseline to 12 months
Title
Cost Effectiveness
Description
A modified version of the Client Service Receipt Inventory (CSRI; Beecham & Knapp, 2001): to measure costs, service utilisation, income and related matters to analyse cost effectiveness.
Time Frame
Baseline to 12 months
Title
Qualitative Interviews
Description
Explore reasons why individuals may or may not engage with the study and the PS CBT intervention
Time Frame
Baseline to 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
>2 self-harm episodes.
With high levels of unipolar depressive symptoms (BDI-2 score of 17 or more).
Sufficient understanding of English (spoken and written).
Ability to give informed consent
Exclusion Criteria:
Clinical judgement of high level of suicide risk, other risk to self or others requiring other urgent approaches e.g. admission to mental health unit.
Other severe mental illness e.g. psychosis, bipolar disorder, substance use disorder or organic mental disorder e.g. secondary to head injury as the primary mental health problem as determined by a structured psychiatric interview (SCID).
Currently receiving structured psychological therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kapil Sayal, PhD
Organizational Affiliation
CLAHRC-EM, University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
Derbyshire Healthcare NHS Foundation Trust
City
Derby
State/Province
Derbyshire
ZIP/Postal Code
DE22 3LZ
Country
United Kingdom
Facility Name
Derbyshire Hoispitals NHS Foundation Trust
City
Derby
State/Province
Derbyshire
ZIP/Postal Code
DE22 3NE
Country
United Kingdom
Facility Name
Chesterfield Royal Hospital NHS Foundation Trust
City
Chesterfield
State/Province
Deryshire
ZIP/Postal Code
S44 5BL
Country
United Kingdom
Facility Name
Nottinghamshire Healthcare NHS foundation Trust.
City
Nottingham
State/Province
Nottinghamshire
ZIP/Postal Code
NG3 6AA
Country
United Kingdom
12. IPD Sharing Statement
Citations:
Citation
Beck AT. Beck Hopelessness Scale. The Psychological Corporation: San Antonio, Texas, 1988.
Results Reference
background
Citation
Beck AT, Steer RA, Brown GK. Manual for the Beck Depression Inventory-II. San Antonio, TX: Psychological Corporation, 1996.
Results Reference
background
PubMed Identifier
18647396
Citation
Bee PE, Bower P, Lovell K, Gilbody S, Richards D, Gask L, Roach P. Psychotherapy mediated by remote communication technologies: a meta-analytic review. BMC Psychiatry. 2008 Jul 22;8:60. doi: 10.1186/1471-244X-8-60.
Results Reference
background
PubMed Identifier
10109801
Citation
EuroQol Group. EuroQol--a new facility for the measurement of health-related quality of life. Health Policy. 1990 Dec;16(3):199-208. doi: 10.1016/0168-8510(90)90421-9.
Results Reference
background
PubMed Identifier
22278284
Citation
Whittaker R, Merry S, Stasiak K, McDowell H, Doherty I, Shepherd M, Dorey E, Parag V, Ameratunga S, Rodgers A. MEMO--a mobile phone depression prevention intervention for adolescents: development process and postprogram findings on acceptability from a randomized controlled trial. J Med Internet Res. 2012 Jan 24;14(1):e13. doi: 10.2196/jmir.1857.
Results Reference
background
PubMed Identifier
33884617
Citation
Witt KG, Hetrick SE, Rajaram G, Hazell P, Taylor Salisbury TL, Townsend E, Hawton K. Psychosocial interventions for self-harm in adults. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013668. doi: 10.1002/14651858.CD013668.pub2.
Results Reference
derived
PubMed Identifier
30678674
Citation
Sayal K, Roe J, Ball H, Atha C, Kaylor-Hughes C, Guo B, Townsend E, Morriss R. Feasibility of a randomised controlled trial of remotely delivered problem-solving cognitive behaviour therapy versus usual care for young people with depression and repeat self-harm: lessons learnt (e-DASH). BMC Psychiatry. 2019 Jan 24;19(1):42. doi: 10.1186/s12888-018-2005-3.
Results Reference
derived
Links:
URL
http://www.clahrc-em.nihr.ac.uk/clahrc-em-nihr/research/enhancing-mental-health/edash-study.aspx
Description
CLAHRC-East Midlands Website: eDASH Study
Learn more about this trial
RCT of the Clinical and Cost Effectiveness of Cognitive Behaviour Therapy (CBT) Delivered Remotely Versus Treatment as Usual in Adolescents and Young Adults With Depression Who Repeatedly Self-harm
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