ANZCTR - Registration

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Trial registered on ANZCTR

Registration number

ACTRN12617000024347

Ethics application status

Approved

Date submitted

22/12/2016

Date registered

9/01/2017

Date last updated

31/05/2024

Date data sharing statement initially provided

21/10/2021

Type of registration

Prospectively registered

Titles & IDs

Public title

Activation Therapy for the Treatment of Inpatient Depression

Scientific title

Randomised controlled trial of Activation Therapy versus Treatment As Usual for the treatment of cognitive impairment in inpatients admitted with depression

Secondary ID [1]

Nil known

Universal Trial Number (UTN)

U1111-1190-9517

Trial acronym

Linked study record

Health condition

Health condition(s) or problem(s) studied:

Depression

Condition category

Condition code

Mental Health

Depression

Intervention/exposure

Study type

Interventional

Description of intervention(s) / exposure

8 x 30-40 minute therapist sessions of Activation Therapy on-site at the psychiatric unit (4/week) and 10 x online practise sessions over 2 weeks (5/week) in addition to Treatment as Usual (see comparator treatment).

Activation Therapy consists of two components. Cognitive Activation and Behavioural Activation.

Cognitive Activation is the use of therapist guided computerised cognitive exercises from a programme called Scientific Brain Training Pro (https://www.scientificbraintrainingpro.com/ - provided free of charge for this study). These exercises are designed to activate parts of the brain that are under-active with depression. This system has been selected based on its use of tasks with flexibility to alter level of difficulty to meet the individual’s current functioning, ease of use and delivery in an attractive interactive format. Therapists will select cognitive tasks suitable for the patient’s current level of functioning from a menu of tasks, and in later sessions, review progress. Collaborative practice, encouragement and coaching will take place. Therapists will be experienced registered nurses, social workers, or psychologists familiar with the requirements of ward environments and working within multi-disciplinary teams. Patients will be encouraged to practise the exercises in-between therapy sessions to reinforce and build on learning occurring during therapy. Patients will focus on the exercises used in therapy when doing the on-line practise sessions.

Behavioural Activation occurs alongside the Cognitive Activation in the therapy led sessions. Behavioural Activation involves identification of both positive and negative reinforcers maintaining depressive symptoms and behaviours, and of reinforcers that promote more adaptive behaviours (i.e. those that re-engage the depressed person with previously rewarding or potentially rewarding aspects across the important domains of life). Personal values are identified and activities focussed on those values are considered. A graded hierarchy of pleasurable activities and activities that give the patient a sense of competency is then chosen and worked through collaboratively with the patient. Collaborative problem-solving of difficulties in undertaking the tasks occurs.

Training/adherence
Activation Therapy will be delivered according to our Activation Therapy manual by mental health professionals trained and closely supervised with a focus on adherence and competence.
Fidelity checklists of core strategies delivered during each sesson will be completed by therapists after each session to ensure all elements are delivered.
A random selection of 10% of audiotaped sessions will be listened to by a supervisor and scored according to the Quality of Behavioral Activation Scale.
Participant adherence will be measured by the 9-item Short Form Behavioral Activation Scale (BADS-SF) completed by participants at baseline, session 4 and session 8.
A single question self-rating the extent of practice of Behavioural Activation activities within the past 24 hours will be completed by participants at each session. The frequency and duration of on-line cognitive activation exercises will also be monitored through the Scientific Brain Training Pro programme.

Intervention code [1]

Treatment: Other

Comparator / control treatment

Treatment as Usual involves nursing care, regular review with medical staff, pharmacotherapy, and an occupational therapist led therapeutic programme including diversional group activities (walks and therapeutic activities e.g., cooking). Availability of psychology input is limited due to resourcing factors and usually only occurs in cases in which the admission has become prolonged and would therefore occur after the end of the treatment period. Treatment as Usual is provided for the study period (2 weeks) and then continues for patients in the comparator and intervention groups until discharge.

Control group

Active

Outcomes

Primary outcome [1]

Rates of hospital re-admission within 12 weeks of discharge – these will be determined from the patient’s electronic record and it is therefore very unlikely that there will be any missing data for this outcome.

Timepoint [1]

12 weeks following discharhge

Primary outcome [2]

Timepoint [2]

12 weeks following discharge

Secondary outcome [1]

Change in the Functioning Assessment Short Test will be used to assess functioning

Timepoint [1]

14 weeks after baseline assessment

Secondary outcome [2]

The Montgomery Asberg Depression Rating Scale (MADRS) is a clinician-rated depression severity scale which will be used to assess depression severity.

Timepoint [2]

2 weeks, 8 weeks, and 14 weeks following baseline assessment

Secondary outcome [3]

Readmission to hospital with a primary diagnosis of depression will be assessed by a review of medical records

Timepoint [3]

within 1 year following baseline assessment

Secondary outcome [4]

Total days spent in hospital will be assessed by a review of medical records

Timepoint [4]

within 1 year following baseline assessment

Secondary outcome [5]

Change in a composite cognitive score generated by adding z scores of the change between baseline and follow-up for a pre-selected group of cognitive measures. These measures cover the domains of visual and verbal memory and learning, attention, executive function, and psychomotor function. The composite score measures are comprised from the following variables: Brief Visuospatial Memory Test, Rey Auditory-Verbal Learning Task- total words recalled in all learning trials, Rey Auditory-Verbal Learning Task - words recalled delayed recall, Category Fluency- total words generated, Category Fluency Switching - total correct switches, Digit Span - total forwards plus backwards, Trail Making Test part A and B, Stroop Test, Symbol Coding (BACS). The composite score will be calculated by computing z scores for each variable (score/standard deviation of the score at baseline). The z score for each variable will be added and divided by the number of variables to create a composite z score. z scores at baseline and at follow-up will be entered into general linear model.

Timepoint [5]

14 weeks

Eligibility

Key inclusion criteria

Individuals admitted to the participating psychiatric inpatient units with a primary diagnosis of depression, who are computer literate and able to complete questionnaires and therapy in English.

Minimum age

18 Years

Maximum age

65 Years

Sex

Both males and females

Can healthy volunteers participate?

Key exclusion criteria

Primary diagnosis of schizophrenia
Current severe alcohol or drug use disorder
Comorbid serious endocrinological, neurological or chronic medical condition
Pregnancy
Previous severe head injury
Electro-convulsive therapy (ECT) in the past six months or ECT planned for the current admission

Study design

Purpose of the study

Treatment

Allocation to intervention

Randomised controlled trial

Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)

Randomisation will occur after consent and baseline measures. Randomisation will be undertaken by the research nurse accessing a password protected on-line system.

Methods used to generate the sequence in which subjects will be randomised (sequence generation)

Computer generated permuted block, stratified by mood disorder diagnosis (bipolar vs unipolar) and by treatment unit (te Awakura in-patient unit vs Te ao Marama in patient unit)

Masking / blinding

Blinded (masking used)

Who is / are masked / blinded?

The people assessing the outcomes

Intervention assignment

Parallel

Other design features

Phase

Not Applicable

Type of endpoint/s

Efficacy

Statistical methods / analysis

The primary outcome will be analysed by Cochrane Mantel-Haenszel Test, stratified by site and mood disorder diagnosis. The analysis population will be intention-to-treat.

The 12 week re-admission rate between 2013 and 2015 (prior to the start of the feasibility study) was 40%. We propose that a clinically significant reduction in this rate would be to 20%. To have 80% power to show such a difference between groups as statistically significant (p<0.05) will require 82 patients per group.

The power calculation for the secondary outcome of composite cognitive measure will be as follows. In an equivalent group of patients with depression, the difference in mean z-scores between patients and healthy controls on the composite cognitive measure at follow-up was 0.8. We can therefore assume a similar difference in the TAU group. A clinically meaningful difference would be to reduce this by half - to a difference after treatment of 0.4 in the AT group. The SD of change of the composite z-score in the equivalent group was 0.7. We are therefore aiming for a difference in change in z-score compared with controls of 0.4 with an SD of 0.7. Sixty five patients per group will give 90% power to detect this difference as statistically significant (2-tailed a=0.05).

This secondary outcome will be analysed by general linear mixed model with group and site as between-subject factors and time (baseline/follow-up) as a within-subjects factor. Analysis population will be intention-to-treat with all patients who are randomised entered into the analysis. This will be regardless of protocol (treatment adherence). Patients who do not undergo repeat cognitive testing will be assumed not to have changed. Close liaison with patients and their clinicians following discharge and an interim contact to carry out mood rating, plus testing in patients’ homes will maximise follow-up and minimise the chance of differential dropout between groups.

Recruitment

Recruitment status

Active, not recruiting

Date of first participant enrolment

Anticipated

3/09/2018

Actual

4/02/2019

Date of last participant enrolment

Anticipated

2/07/2023

Actual

27/07/2023

Date of last data collection

Anticipated

27/07/2024

Actual

Sample size

Target

170

Accrual to date

Final

Recruitment outside Australia

Country [1]

New Zealand

State/province [1]

Canterbury, South Canterbury

Funding & Sponsors

Funding source category [1]

Charities/Societies/Foundations

Name [1]

Canterbury Medical Research Foundation

Address [1]

Level 1/230 Antigua St, Christchurch Central, Christchurch 8011

Country [1]

New Zealand

Funding source category [2]

Government body

Name [2]

New Zealand Health Research Council

Address [2]

Level 3, ProCare Building, 110 Stanley Street, Auckland 1010, PO Box 5541, Wellesley Street, Auckland 1141, NZ

Country [2]

New Zealand

Primary sponsor type

Individual

Name

Professor Richard Porter

Address

Terrace House
PO Box 4345
Christchurch Mail Centre
Christchurch 8140

Country

New Zealand

Secondary sponsor category [1]

None

Name [1]

None

Address [1]

None

Country [1]

Ethics approval

Ethics application status

Approved

Ethics committee name [1]

Health and Disabilities Ethics Committees (Northern B Health and Disability Ethics Committee

Ethics committee address [1]

Ministry of Health, P.O. Box 5013, Wellington 6140, NZ.
Physical Address: 133 Molesworth St., Thorndon, Wellington 6011, NZ

Ethics committee country [1]

New Zealand

Date submitted for ethics approval [1]

09/04/2018

Approval date [1]

01/06/2018

Ethics approval number [1]

18/NTB/75

Summary

Brief summary

Depression is a common and serious problem. Patients who are admitted for treatment of depression are generally the most severely affected with the greatest degree of depressive and cognitive symptoms (difficulty with thinking, memory, and organising).

Existing treatments of depression largely consist of medications and psychotherapies (talking treatments). However, these treatments are limited for a number of reasons including partial response rates (not helping everybody who takes the treatment), incomplete responses (only improving depression somewhat), and persisting cognitive symptoms despite improvements in mood. These factors are all linked to poor functional recoveries (failure to return to previous level of functioning) and risk of depression returning.

Current treatment of depression on a psychiatric ward largely provides a secure setting that minimises the risk of suicide whilst medications take effect. Unfortunately, the evidence for non-medication strategies to improve the care of inpatients with depression is not well established and largely preliminary in its findings. This study, therefore, seeks to improve the evidence base for non-medication strategies for inpatients with depression. 

Behavioural Activation is a treatment that has predominantly been studied in outpatient depression studies with good evidence for its effectiveness. Behavioural Activation helps people by assisting them to increase their activity levels. Cognitive Activation is a new treatment that is increasingly being evaluated for depression and other mental disorders. Cognitive activation stimulates under-active areas of the brain with on-line computer games. We have combined Behavioural Activation and Cognitive Activation to create Activation Therapy (AT). We believe that this combination of treatments provides the best chance of helping people with severe inpatient depression. 

Our study will assess whether AT given in addition to usual treatment (Treatment As Usual (TAU)) on a psychiatric ward is better than TAU for inpatients with depression. If patients agree to participate in the study, they will be randomly chosen to either have Activation Therapy and TAU or TAU alone. 

Our main goal is to assess whether or not Activation Therapy will reduce re-admission to hospital in the 12 weeks following discharge. We will also measure cognitive function, symptoms of depression, functioning, and total time spent in hospital to help us understand if Activation Therapy is useful for inpatients with depression.improves the cognitive deficits caused by depression.

Trial website

Trial related presentations / publications

Public notes

Contacts

Principal investigator

Name

Prof Richard Porter

Address

Department of Psychological Medicine
University of Otago, Christchurch
PO Box 4345
Christchurch Mail Centre
Christchurch 8140

Country

New Zealand

Phone

+64 3 3726700

Fax

+64 3 3726707

richard.porter@otago.ac.nz

Contact person for public queries

Name

Richard Porter

Address

Department of Psychological Medicine
University of Otago, Christchurch
PO Box 4345
Christchurch Mail Centre
Christchurch 8140

Country

New Zealand

Phone

+64 3 3726700

Fax

+64 3 3726707

richard.porter@otago.ac.nz

Contact person for scientific queries

Name

Richard Porter

Address

Department of Psychological Medicine
University of Otago, Christchurch
PO Box 4345
Christchurch Mail Centre
Christchurch 8140

Country

New Zealand

Phone

+64 3 3726700

Fax

+64 3 3726707

richard.porter@otago.ac.nz

Data sharing statement

Will individual participant data (IPD) for this trial be available (including data dictionaries)?

No/undecided IPD sharing reason/comment

What supporting documents are/will be available?

No Supporting Document Provided

Results publications and other study-related documents

Documents added manually

No documents have been uploaded by study researchers.

Documents added automatically

Source	Title	Year of Publication	DOI
Embase	Activation therapy for the treatment of inpatients with depression - Protocol for a randomised control trial compared to treatment as usual.	2019	https://dx.doi.org/10.1186/s12888-019-2038-2

N.B. These documents automatically identified may not have been verified by the study sponsor.

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Documents added automatically