Is mindfulness-based cognitive therapy a feasible additional treatment for young people who do not completely recover from depression after treatment at Child and Adolescent Mental Health Services or who rapidly get depressed again?
| ISRCTN | ISRCTN17823155 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN17823155 |
| IRAS number | 285257 |
| Secondary identifying numbers | IRAS 285257 |
- Submission date
- 26/08/2020
- Registration date
- 04/09/2020
- Last edited
- 16/08/2022
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Mental and Behavioural Disorders
Plain English summary of protocol
Background and study aims
Depression affects people in different ways and can cause a wide variety of symptoms. They range from lasting feelings of unhappiness and hopelessness to losing interest in the things you used to enjoy and feeling very tearful. Many people with depression also have symptoms of anxiety. There can be physical symptoms too, such as feeling constantly tired, sleeping badly, having no appetite or sex drive, and various aches and pains.
Depression in teenagers knocks normal development off course and disrupts family relationships. Even after treatment, many young people are left with depressive symptoms, so we need more treatments for this group who suffer greatly. We have developed a new treatment; Mindfulness for Adolescents and their Carers (MAC), which helps young people and their parents to learn to recognise unhelpful patterns of thoughts, feelings and behaviours, and to find alternative ways to cope with distress. Our earlier work shows that young people and their parents wanted to attend MAC sessions, which they found helpful. Young people's depressive symptoms reduced afterwards.
Aims
Before we can test whether MAC works and is value for money, we need to answer three questions.
1. Who should be trained to deliver MAC, and how should they be trained?
2. What does usual treatment look like for this group of young people?
3. What is the best way to recruit young people and their carers to trial of MAC?
Who can participate?
1. Young people aged 14-17 with a primary clinical diagnosis of depression who have had initial treatment at Child and Adolescent Mental Health Services (CAMHS) and are not fully recovered or who have relapsed quickly following discharge, and their parent(s) / carer(s)
2. CAMHS practitioners at band 6 or above with a personal mindfulness practice and level 1 training in mindfulness-based intervention delivery, or equivalent experience
What does the study involve?
1. We will develop a training programme for potential group leaders who will attend 4 days of training prior to delivering MAC under supervision
2. We will interview key managers and practitioners in CAMHS about the depression treatment pathway and carry out a detail study of records to understand usual treatment for this group of young people.
3. We will run two groups of 10 young people (with a parallel group for their parents/ carers) to establish whether we can recruit and retain effectively and to study which questionnaires work best for a future randomised controlled trial. There are 9 weekly workshops, each lasting 1.5 hours. Workshops will be held using NHS approved video conferencing software that can be accessed securely from participants’ homes using a laptop/computer or smart phone
4. We will ask both young people and their parent or carer to fill in a set of questionnaires at three different times, when they join the study at baseline and then 4 and 9 months later. The questions will help us to measure if there have been any changes in the way participants are feeling. These questions will be completed on a secure online website which participants can access via a computer or smart phone. These questionnaires are likely to take about 90 minutes to complete.
What are the possible benefits and risks of participating?
The young people and parents who participate will get access to a novel treatment that shows promise in young people and is established in adults.
The practitioners attending training will develop new skills and a deeper understanding of mindfulness.
All participants will need to complete questionnaires and some will discuss their experiences in person. This will demand their time, and some of the topics may be sensitive for some people. The researchers will do their utmost to avoid distress and anyone who becomes distressed will be signposted to support.
Mindfulness techniques can increase anxiety or lead to distress in some people. Group leaders will be trained to identify and support any young people or parents who experience such distress and support will be provided.
Where is the study run from?
University of Cambridge (UK)
When is the study starting and how long is it expected to run for?
May 202 to September 2021
Who is funding the study?
National Institute for Health Research Programme Development Grants (UK)
Who is the main contact?
Prof. Tamsin Ford, tjf52@medschl.cam.ac.uk
Contact information
Scientific
Department of Psychiatry
Douglas House
18b Trumpington Road
Cambridge
CB2 2AH
United Kingdom
 ORCID ID |
0000-0001-5295-4904 |
|---|---|
| Phone | +44 (0)7891 409229 |
| tjf52@medschl.cam.ac.uk |
Study information
| Study design | Multi-centre mixed methods feasibility study |
|---|---|
| Primary study design | Observational |
| Secondary study design | Mixed qualitative and quantitative study to evaluate the feasibility of training therapists and recruiting and retaining 20 young people and their carers including randomised allocation to MBCT or treatment as usual |
| Study setting(s) | Other |
| Study type | Treatment |
| Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet |
| Scientific title | A combined mindfulness-based approach for adolescent non-responders to first-line treatments of depression and their carers: establishing feasibility of implementation and delivery |
| Study acronym | ATTEND |
| Study objectives | This proposal addresses four important uncertainties and will: 1. Develop the training programme for therapists, which may need to differ in emphasis depending on whether they come from child mental health or mindfulness backgrounds 2. Describe current care pathways (to aid recruitment) and develop an understanding of what Treatment As Usual (TAU; probable comparator) comprises for the young people we want to recruit 3. Test the process for identifying young people and their carers and see how many start and finish MAC, so we better understand how many clinics we need to work with to test MAC in a definitive trial 4. Test the acceptability of asking for blood and saliva samples for the future study of how MAC works |
| Ethics approval(s) | Approved 10/12/2020, Cambridgeshire South REC (Level 3, Block B, Whitefriars, Lewins Mead, Bristol, BS1 2NT, UK; +44 (0)207 104 8134; cambridgesouth.rec@hra.nhs.uk), ref: 20/EE/0246 |
| Health condition(s) or problem(s) studied | Depression |
| Intervention | Potential therapists will attend 4 days of training to be delivered remotely to familiarise them with the manual – they will then contribute to the delivery of MBCT to two groups of 10 young people or the parallel groups for their carers ‘Mindfulness for Adolescents and Carers’ (MAC) is delivered to a group of up to 10 young people at a time, there are 9 weekly workshops, each lasting 1.5 hours. Workshops will be held using NHS approved video conferencing software that can be accessed securely from participants’ homes using a laptop/computer or smart phone. Their parent or carer are invited to attend a parallel but separate workshop with other carers to work through similar materials. Both young people and their parent or carer fill in a set of questionnaires at three different times, when they join the study at baseline and then 4 and 9 months later. |
| Intervention type | Behavioural |
| Primary outcome measure | All outcomes are measured at baseline and then 4 and 9 months later. The following constructs will be measured in young people using the following measures: 1. Depression using RCADS 2. Quality of Life using CHU-9D 3. Family dynamics using Score-15 4. Mindfulness using CAMM 5. Self-compassion using SCS-SF 6. Emotional Regulation using ERQ 7. Decentering using EQ (Decentering Scale) 8. Rumination using CRSQ And in parents/carers: 9. Depression using GAD and PHQ-9 10. Quality of Life using EQ-5D 11. Family dynamics using Score-15 12. Mindfulness using FFMQ-SF 13. Self-compassion using SCS-SF 14. Emotional Regulation using ERQ 15. Decentering using EQ (Decentering Scale) 16. Rumination using RRS |
| Secondary outcome measures | There are no secondary outcome measures |
| Overall study start date | 01/05/2020 |
| Completion date | 30/09/2021 |
Eligibility
| Participant type(s) | Mixed |
|---|---|
| Age group | Child |
| Lower age limit | 14 Years |
| Upper age limit | 17 Years |
| Sex | Both |
| Target number of participants | 40 young people with one or both parents - 20 in each site |
| Key inclusion criteria | Young People: 1. CAMHS patients with a primary diagnosis of depression 2. Aged 14 - 17 years at the time of recruitment 3. Completed at least one NICE recommended treatment for depression or anxiety 4. Not recovered sufficiently to be discharged, or who have subsequently relapsed and been re-referred 5. Scoring 60 or more on the self-report RCADS Carers: 6. A carer of a young person who has consented to take part in the study Group leaders: 7. Band 6 and above with professional training meaning they can work therapeutically with depressed (and anxious) CYP 8. A named CAMHS service senior clinician to support clinician delivering the group with risk – Clinical responsibility rest with CAMHS 9. Own personal mindfulness practice following attendance at either 8-week MBCT or MBSR group 10. Some experience of leading or co-leading an MBI but ideally level 1 teacher training |
| Key exclusion criteria | Young People: 1. A primary presenting problem of eating disorder, post-traumatic stress disorder or psychosis 2. Self-harming behaviour or substance misuse necessitating current active clinical management |
| Date of first enrolment | 15/01/2021 |
| Date of final enrolment | 22/03/2021 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centres
Douglas House, 18b Trumpington Road
Cambridge
CB28AH
United Kingdom
Magdelen Road
Exeter
EX12LU
United Kingdom
16 De Crespigny Park
Camberwell
London
SE5 8AF
United Kingdom
4 Huxley Road
The Surrey Research Park
Guildford
GU2 7RE
United Kingdom
Sponsor information
Hospital/treatment centre
Elizabeth House
Fulbourn Hospital
Cambridge
CB21 5EF
England
United Kingdom
| Phone | +44 (0)1223 219400 |
|---|---|
| r&d@cpft.nhs.uk | |
| Website | http://www.cpft.nhs.uk/ |
"ROR" |
https://ror.org/040ch0e11 |
Funders
Funder type
Government
Government organisation / National government
- Alternative name(s)
- NIHR Programme Development Grants, NIHR – Programme Development Grants, PDG
- Location
- United Kingdom
Results and Publications
| Intention to publish date | 31/12/2021 |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not expected to be made available |
| Publication and dissemination plan | We anticipate the following outputs from this study • PGfAR application (all – TF lead) • Protocol for RCT (all RH to lead drafting – draw in stats and health economics) • Treatment Recording Scale / equivalent that is validated • MAC manuals (as IP for the bid, with additions from this work is necessary) • MAC training and delivery manuals finalised but to be published on completion of the main trial (TB, PS, JR, JF) Academic papers:- • Conceptual paper about how the manual has been modified in the light of the current literature in order to optimise response • Intervention mapping paper • Current state of provision for young people with depression |
| IPD sharing plan | The datasets generated during and/or analysed during the current study are not expected to be made available due to confidentiality. |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Plain English results | 01/11/2020 | 09/08/2022 | No | Yes | |
| Results article | 01/11/2020 | 09/08/2022 | Yes | No | |
| Protocol file | version 1.3 | 06/04/2021 | 16/08/2022 | No | No |
| HRA research summary | 28/06/2023 | No | No |
Additional files
Editorial Notes
16/08/2022: Uploaded protocol (not peer-reviewed) as an additional file.
09/08/2022: The following changes were made to the trial record:
1. Publication reference added.
2. Link to plain English results added.
27/01/2021: The following changes were made to the trial record:
1. The recruitment start date was changed from 10/12/2020 to 15/01/2021.
2. The recruitment end date was changed from 31/01/2021 to 22/03/2021.
16/12/2020: The ethics approval was added.
15/12/2020: The following changes were made to the trial record:
1. The IRAS number was added to the Protocol /serial number field.
2. The recruitment start date was changed from 01/11/2020 to 10/12/2020.
3. The recruitment end date was changed from 31/12/2020 to 31/01/2021.
28/08/2020: Trial’s existence confirmed by National Institute for Health Research (NIHR)
