MAPS: Mood Awareness Psychotherapy Support

Sponsor
University College, London (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06133582
Collaborator
Linköping University, Sweden (Other)
80
2
9.2

Study Details

Study Description

Brief Summary

The aim of this mixed-methods, two arm, randomised waitlist control feasibility trial is to examine an internet delivered, self-help program for depression and anxiety, based on psychodynamic therapy. The study will compare two conditions: the psychodynamic program with therapist support, and a waitlist control. The participants will be university students.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Internet Based Psychodynamic Psychotherapy
N/A

Detailed Description

Background: There appears to be an increase in mental health difficulties amongst higher education students in the UK. However, NHS services are over-stretched, and clients often experience long waits for treatment, during which time their symptoms may worsen. Internet-based therapies could be an important and accessible treatment option, particularly when provided within the context of the university, as this has the potential to provide timely treatment to those seeking help.

The majority of internet-based therapies use a Cognitive Behavioural Therapy framework. However, psychodynamic therapy has also been adapted to an internet-based format - often called 'iPDT'. One such iPDT programme was developed in Sweden for the treatment of adolescent depression. This is a self-guided programme, with therapist support. Clients 'chat' with their therapist once a week, for 30-minutes, using an instant-messaging platform on the therapy website. They can also send a-synchronous messages to their therapist, and the therapist can view the worksheets that client's complete on the therapy website.

This iPDT programme has been evaluated in two Randomised Controlled Trials, both of which showed it to be effective. Given the promising results of the Swedish iPDT programme, a research team at the Anna Freud Centre in the UK conducted a pilot study of an English-language version of the treatment; this pilot found evidence of a decrease in adolescents' symptoms of depression, and an improvement in emotion regulation, at the end of the 10-week treatment, with outcomes maintained at three month follow up.

At present, we do not know whether the iPDT programme would be accepted by, and effective for, participants without the weekly instant-messaging sessions. These 'chat sessions' are valued by many service users, but increase the cost and intensity of the programme. Furthermore, to date, the English-language version of the programme has not been tested with a university student population - young adults, rather than adolescents.

Study aims and design: This will be a mixed-methods, two arm, randomised waitlist control feasibility trial. We aim to recruit approximately 80 university students with symptoms of depression and anxiety.

The aims of the study are to assess recruitment and retention rates of participants, including at three month follow up. To examine acceptability of the platform for the new target population, including levels of engagement with different elements of the treatment across the course of the intervention. The study will also explore indications of treatment efficacy. Additional exploratory analyses will be undertaken to explore moderators and mediators of change.

Participants in the treatment arm will receive Internet Based Psychotherapy (iPDT). This is a 10-week intervention, delivered on the therapy website - called 'Iterapi' - which was developed at Linköping University in Sweden. The programme involves creative and interactive web-based content: worksheets, audio, video, expressive writing exercises. Additionally, each participant is assigned a Therapeutic Support Worker (TSW). The TSW logs into the platform and views the questionnaires and other data provided by the participants that they are supporting. Each week, the TSW sends each of their participants a reflective message in response to the data they have provided when interacting with the programme over the last week. The participant can reply to this message.

After completing the 10 week intervention, qualitative data will be collected via interviews with some participants to explore participants' experiences of the IPDT programme, in particular focussing on therapy process and their understandings of mechanisms of change, and of 'what works for whom'. Participants will also complete a set of follow up questionnaires 3 months after they complete the intervention.

The iPDT programme has 8 chapters. The principal objective of the iPDT intervention is to reduce depressive symptoms through the promotion of emotional awareness and emotional experience. The intervention is an affect-focused therapy and draws on Malan's Triangle of Conflict. Participants are invited to link their emotions to depressive symptoms, to challenge defences, regulate anxiety, and explore previously avoided feelings.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Mood Awareness Psychotherapy Support - A Randomised Feasibility Trial of an Internet-Based Psychodynamic Treatment for University Students With Low Mood
Anticipated Study Start Date :
Nov 27, 2023
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Internet-Based Psychodynamic Psychotherapy

Participants received the internet-based intervention for 10 weeks, supported by messages from their Therapeutic Support Worker.

Behavioral: Internet Based Psychodynamic Psychotherapy
This is a 10-week intervention, delivered on a website called 'Iterapi' which was developed in Sweden. The programme involves creative and interactive web-based content- worksheets, audio, video, expressive writing exercises. Additionally, each participant is assigned a Therapeutic Support Worker (TSW). The TSW logs into the platform and views the questionnaires and other data provided by the participants that they are supporting. Each week, the TSW sends each of their participants a reflective message in response to the data they have provided when interacting with the programme over the last week. The participant can reply to this message. The principal objective of the iPDT intervention is to reduce depressive symptoms through the promotion of emotional awareness and emotional experience. The intervention is an affect-focused therapy and draws on Malan's Triangle of Conflict (Malan, 1995).

No Intervention: Waitlist Control

Participants will receive no intervention for 10 weeks

Outcome Measures

Primary Outcome Measures

  1. Quick Inventory of Depressive Symptomatology - Self Report (QIDS-SR) [Change from baseline to post-treatment (10 week) and follow up at 3 months after treatment (participants complete the measure weekly throughout the intervention)]

    The 16-item QIDS-SR measures depressive symptoms. Scores range from 0-27, higher scores indicate more severe depression.

Secondary Outcome Measures

  1. Generalised Anxiety Disorder Questionnaire (GAD-7) [Change from baseline to post-treatment (10 week) and follow up at 3 months after treatment (participants complete the measure weekly throughout the intervention).]

    The GAD-7 features seven items for assessing anxiety and screening for generalized anxiety disorder. Scores range from 0-21, higher scores indicate more severe anxiety.

  2. Patient Health Questionnaire (PHQ-9) [Change from baseline to post-treatment (10 week) and follow up at 3 months after treatment. (Participants complete the measure at baseline, week 5, week 10, and follow up at 3 months).]

    The PHQ-9 features nine items for assessing depression. Scores range from 0-27, higher scores indicate more severe depression.

  3. Defences Questionnaire DMRS-SR-30 [Change from baseline to post-treatment (10 week) and follow up at 3 months after treatment. (Participants complete the measure at baseline, week 5, week 10, and follow up at 3 months).]

    30-item self-rated measure of psychological defences

Other Outcome Measures

  1. The Working Alliance Inventory for guided Internet interventions (WAI-I) [Participants complete this measure at weeks 2, 3, 4, 5, 6, 7, 8, 9, & 10.]

    12-item self-rated measure of working alliance. Scores range from 12-60, higher scores indicate a stronger alliance.

  2. Depressive Experiences Questionnaire (DEQ English version) [Participants complete this at baseline, week 10, and 3 month follow up.]

    66-item self-report questionnaire designed to differentiate between dependency and self-criticism in people experiencing depression.

  3. Attitudes towards Psychological Online Interventions-the APOI [Participants complete this at baseline, week 10, and 3 month follow up.]

    16-item self-report questionnaire designed to measure participants' attitudes towards and expectations of psychological online interventions. Higher scores indicate a more positive attitude towards psychological online interventions.

  4. Relationship Styles Questionnaire [Baseline only.]

    This is a self-report questionnaire designed to measure adult attachment style. Participants are presented with a short description of each attachment style (secure, fearful, preoccupied, dismissive). They first select which style best matches their own, and then rate each style on a likert scale from 1 - 7, where 1 is very unlike their relationship style, and 7 is very similar to their relationship style.

  5. The Post Study System Usability Questionnaire (PSSUQ) - with minorly adapted wording to suit the therapy platform [Participants complete this in week 10]

    16-item self-report questionnaire measuring participants' experience of using the therapy platform. Lower scores indicate greater satisfaction with the usability of the platform.

  6. Interview [Participants complete this after week 10, before 3 month follow up.]

    To explore participants' experiences of the IPDT programme, in particular focussing on therapy process and their understandings of mechanisms of change, and of 'what works for whom'.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • score of 10 or more on the QIDS-SR
Exclusion Criteria:
  • Under 18 years of age

  • Not a current student at University College London (UCL)

  • Previous diagnosis of: Bipolar disorder, any personality disorder, Psychosis / Schizophrenia, Post Traumatic Stress Disorder, intellectual disability

  • Not being able to confidently read or write in English

  • No access to a device which can access the internet

  • Previous suicide attempts

  • Current plans to attempt suicide

  • Currently receiving psychological therapy

  • Planning to begin psychological therapy during the duration of the intervention

  • Starting new medication for mood, or using mood-medication inconsistently, over the last 3 months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University College, London
  • Linköping University, Sweden

Investigators

  • Study Chair: Rose Mortimer, University College, London
  • Study Chair: Dominika Iluczyk, University College, London

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University College, London
ClinicalTrials.gov Identifier:
NCT06133582
Other Study ID Numbers:
  • 26049/001
First Posted:
Nov 15, 2023
Last Update Posted:
Nov 18, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 18, 2023