跳至主要内容
临床试验/NCT02186730
NCT02186730已完成不适用

Computerised Intervention/Treatment for Adolescent Depression and Low Mood: Feasibility Phase 2

Leeds and York Partnership NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2014年4月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
48
试验地点
1
主要终点
Changes on the Short Beck Depression Inventory from baseline to 4 and 12 months follow up

研究概览

简要总结

This study forms the second phase of previous work to examine the effectiveness of computerised Cognitive Behaviour Therapy (cCBT) to treat adolescents with low mood/depression.

Depression affects around 2% of adolescents. Antidepressants are not recommended for this age range as a first line treatment because of concerns about their usefulness and side effects. Government guidelines have supported using Cognitive Behaviour Therapy (CBT), which is effective and one of the main treatments recommended for depression. It has been suggested that computerised versions of CBT (cCBT) may be effective for treating depression in young people who may prefer this to seeing a therapist face-to-face, but little research exists to date to support this. This study examines the feasibility of running a large scale randomised controlled trial (RCT) to compare a promising cCBT program (Stressbusters) with self-help websites for adolescents with low mood and depression (LMD).

Eligible and consenting participants will complete several questionnaires to assess their mood before being randomly assigned to either cCBT (Stressbusters) or equivalent access to selected websites providing self help for LMD. Participants will complete further mood questionnaires 4 and 12 months after treatment completion/withdrawal. We have already recruited 97 individuals to this trial but aim to recruit a further 48 participants to collect further information.

We are also keen to find out whether sending participants text messages before sessions and around follow up periods will increase attendance/completion. Therefore all trial participants will receive text messages from the research team during their participation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •12 to 18 years
  • •Low mood/depression
  • •co-morbid physical illness or co-morbid non-psychotic functional disorders, such as anxiety

排除标准

  • •Suicidality
  • •Postnatally depressed
  • •Suffering psychotic symptoms

研究组 & 干预措施

Stressbsuters

Experimental

Computerised Cognitive Behaviour package consisting of eight 30-45 minute sessions of CBT designed for 12-18 year olds. Each Stressbusters session is an interactive presentation featuring narration synchronised with videos, animations, graphics and printouts.

The programme has a narrator guiding individuals through each of the eight sessions in a linear progression. Each session builds on the knowledge gained in previous sessions and on tasks carried out at home. Sessions contain flexible "add-ons" such as written fact sheets (for example about bullying, sleep problems) which can be printed out and taken away together with home practice related handouts from the programme (for example mood diary sheets). Session topics include getting activated, relapse prevention, challenging negative thoughts and problem solving

干预措施: Stressbusters (Behavioral)

Websites

Active Comparator

Any individuals randomised to arm 2 of the trial will spend the equivalent time accessing currently available self help websites that provide information about low mood/depression. These four websites will be the same as those used in our initial feasibility study of which, based on our preliminary data, there is evidence for their usefulness.

干预措施: Websites (Behavioral)

结局指标

主要结局

Changes on the Short Beck Depression Inventory from baseline to 4 and 12 months follow up

时间窗: baseline, 4 months follow up, 12 months follow up

次要结局

  • The Short Mood and Feelings Questionnaire(up to 8 weeks)
  • Changes in health status measured by the EQ-5D-Y from baseline to 4 and 12 months follow up(Baseline, 4 months follow up, 12 months follow up)
  • Changes in health status measured by the HUI2 from baseline to 4 and 12 months follow up(Baseline, 4 months follow up and 12 months follow up)
  • Changes on the Mood and Feelings Questionnaire from baseline to 4 and 12 months follow up(Baseline, 4 months follow up, 12 months follow up)
  • Changes on the Spence Children's Anxiety Scale from baseline to 4 and 12 months follow up(Baseline, 4 months follow up and 12 months follow up)
  • The number of health services used by participants between baseline, 4 months and 12 months follow up(Baseline, 4 months follow up, 12 months follow up)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Computerised Intervention/Treatment for Adolescent... | 临床试验