Acceptance and Commitment Therapy for Older Adults

Sponsor
University of Lincoln (Other)
Overall Status
Completed
CT.gov ID
NCT04280445
Collaborator
(none)
3
1
1
7.7
0.4

Study Details

Study Description

Brief Summary

Title: Acceptance and Commitment Therapy for older adults experiencing psychological distress: A hermeneutic single case efficacy design (HSCED) series.

Anxiety and depression in older age is associated with increased level of disability and lower quality of life (OAs). Unfortunately, pharmacological treatments are disproportionality relied upon to manage the mental health of OAs. Despite cognitive behaviour therapy (CBT) being the recommended psychotherapy, there is evidence that CBT is less effective for OAs than younger populations.

An alternative treatment, Acceptance and Commitment Therapy (ACT), has been shown to be effective in reducing distress for OAs experiencing physical health difficulties. Several case studies have also indicated that ACT can be effective for OAs with psychological difficulties. ACT aims to change how a person interacts with their thoughts/feelings; to reduce avoidance; and to promote value-focused living.

The study aims to use an adjudicated HSCED to answer the following questions:
  1. Is ACT an effective intervention for older adult clients experiencing psychological distress.

  2. Do meaningful changes occur for client-participants over the course of ACT intervention?

  3. What specific factors (ACT-specific, non-specific, extra-therapeutic) contribute to observed changes?

  4. Are observed changes broadly attributable to the ACT intervention?

  5. What adaptations may facilitate change when using ACT with older adult clients.

For the study, up to four participants will be recruited from an OA community mental health team, each receiving up to 12 individual sessions of ACT. Participants will be required to complete a number of questionnaires throughout the study, including before/after sessions. Post-treatment, there will be a semi-structured 1:1 interview to explore any changes participants experienced, before a six-week follow-up is employed to check stability of change.

Condition or Disease Intervention/Treatment Phase
  • Other: Psychological therapy
N/A

Detailed Description

This study aims to investigate whether Acceptance and Commitment Therapy (ACT) is an effective psychotherapeutic intervention for older adults experiencing psychological distress; what processes contribute towards psychological change; and what adaptations may be required to optimise ACT for older adults. There is currently an over-reliance on pharmacological treatments to manage older adult mental health (Andreescu & Reynolds, 2011), and a lack of inclusion of older adult in efficacy studies of psychological treatments (Gatz, 2006). Cognitive behaviour therapy (CBT) is the most evidence-based psychological treatment for mental health conditions. It emphasises the link between thoughts and feelings, and uses cognitive restructuring to facilitate improvement in psychological symptoms. However, of the studies that have included older adults, there is evidence that CBT has a lower effect size in older adults than with working age adults (Kishita & Laidlaw, 2017). There are a number of possible reasons for this, including a lack of age specific adaptations, the over focus on diagnosis specific treatment protocols in CBT, and the increasing physical and psychological co-morbidity associated ageing.

ACT is a trans-diagnostic approach which aims to promote better living by supporting clients through six key processes (e.g. mindfulness, values). ACT does not aim to reduce distress, rather its goal is to promote better living or a better quality of life despite distress (Hayes, Strosahl & Wilson, 1999). ACT has been shown to have equal or superior efficacy to CBT with a number of psychological and physical health conditions (A-Tjak et al., 2015; Ruiz, 2012). We propose that ACT would be especially suitable for older adult clients due to the high rate of co-morbidity older adults experience and the reduced ability to change aspects of these.

However, there is a lack of understanding about the processes by which ACT works (Öst, 2014). Randomised controlled trails (RCTs) are the standard research methodology to investigate psychotherapy efficacy. Due to the stringent criteria required for RCT analyses, there is a limit to how transferrable the findings of an RCT can be to clinical populations (i.e. heterogenous groups). As such, a hermeneutic single case efficacy design (HSCED) is an ideal methodology to employ to identify what contributes towards change for each client. HSCED benefits from high ecological validity, whilst actively focusing on non-specific factors (components common to all psychotherapies, e.g., therapeutic alliance) and extra-therapeutic factors (components that are not related to the therapy, usually participant factors) to delineate change processes.

The research proposal has been developed as part of a Doctoral Thesis in Clinical Psychology. This involved various research presentations panels and submission of an initial research protocol. These are designed to guide the decision-making process and gain feedback from the course research team. As part of the doctoral program, each trainee is allocated a Primary and Secondary Research Supervisor (both Clinical Psychologists), who aided in shaping the practicalities of this research proposal. Each project also recruits a Field Supervisor who supports with expertise in the project area. Participants will be recruited from the service the Field Supervisor is employed at, thereby creating a direct level of clinical supervision that is paramount to psychotherapy.

Participants will be informed about the study through a member of their healthcare team. The service will ensure potential participants have the capacity to consent to treatment and will provide them with an overview of the study. Potential participants will be made aware of informed consent; that they do not have to take part and that declining to take part will in no way affect their treatment from the service. If a participant declines to take part at this stage, they will be offered treatment as usual from the service. If they consent to take part, the researcher will contact them the following week to answer any additional questions. This will allow them sufficient time to consider whether they would like to take part or not.

This research aims to use a sample that is representative of older adults presenting with psychological distress. See Inclusion/Exclusion sections for further explanation of these criteria.

This study aims to reflect usual clinical practice where possible; therefore, the burden to participants will be of a similar level to treatment as usual. That is, they will be expected to attend the older adults service for regular one-to-one psychotherapy and to discuss their mental health difficulties, contributing factors and what is maintaining their difficulties. Thus, as with any psychological therapy, there is a potential risk that talking about distressing experiences will cause an increase in frequency or intensity of pre-existing mental health conditions. These risks will be monitored through the study by the Trainee Clinical Psychologist (who is both researcher and therapist) through discussion with the participant, use of outcome measures and importantly by utilising weekly clinical supervision with the Clinical Psychologist at the service. This allows a space for any concerns to be raised and for the service to have clinical oversight of the participants.

The aspects of the study which are additional to usual practice are as follows: participants will be required to complete more questionnaires; and participants will be required to come in for an interview after the block of therapy has ended. Every effort has been made to reduce the burden these place upon participants. For instance, shorter questionnaires have been used where possible. Participants will also be asked about any adaptations required to complete questionnaires (e.g. larger font, someone completing questionnaires with them). Participants will be reimbursed for the aspects of the study which are additional to usual practice.

There are several potential benefits to participants taking part in this research, as suggested by the ACT literature. These include decreased psychological distress, increased psychological flexibility and improved quality of life.

To ensure confidentiality, Participant Study Numbers (PSN) will be assigned to each participant to correspond with treatment data. PSNs will be listed in the Trial Recruitment Log along with participant's name, date of birth and NHS number. All other documents related to the participant will use the PSN only. All researchers will endeavour to protect the rights of the participants to privacy and will adhere to the Data Protection Act, 2018. Only the minimum required information for the purposes of the study will be collected. Participant information will be held securely, in a locked room, or locked cupboard or cabinet. Access to the information will be limited to the study staff and investigators. Computer held data including the study database will be held securely and password protected. All data will be stored on a secure dedicated web server. Access will be restricted by user identifiers and passwords (encrypted using a one-way encryption method). Information about the study in the participant's medical records / hospital notes will be treated confidentially in the same way as all other confidential medical information.

As the main researcher is also the therapist, potential conflict of interests will be managed by: using weekly clinical supervision; fortnightly ACT supervision; a 20% random sampling of the audio recorded sessions to ensure adherence to ACT techniques; and using an independent researcher to carry out the Change Interview. Another benefit of using a HSCED series, is that an independent panel adjudicates on the final outcome as to where change was attributed for each client, reducing the researcher-therapist bias.

Study Design

Study Type:
Interventional
Actual Enrollment :
3 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
The study will employ an adjudicated Hermeneutic Single Case Efficacy Design (HSCED) series with three participants. Following Elliott's (2002; Elliott et al., 2009) approach, a crucial aspect of HSCED research is the formation of rich case records. Developed for each client, these consist of data from various time points in the study, and include demographic, quantitative (outcome measures, treatment fidelity measures etc.) and qualitative sources (Change Interview, therapy feedback, therapy process notes and recordings). The rich case records are then cross-referenced and synthesised into an affirmative and sceptic brief. These briefs are then presented to an expert panel to be adjudicated on the process of change. The resulting decisions will then allow for a between-participant analysis of what components contributed towards change and why.The study will employ an adjudicated Hermeneutic Single Case Efficacy Design (HSCED) series with three participants. Following Elliott's (2002; Elliott et al., 2009) approach, a crucial aspect of HSCED research is the formation of rich case records. Developed for each client, these consist of data from various time points in the study, and include demographic, quantitative (outcome measures, treatment fidelity measures etc.) and qualitative sources (Change Interview, therapy feedback, therapy process notes and recordings). The rich case records are then cross-referenced and synthesised into an affirmative and sceptic brief. These briefs are then presented to an expert panel to be adjudicated on the process of change. The resulting decisions will then allow for a between-participant analysis of what components contributed towards change and why.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Acceptance and Commitment Therapy for Older Adults Experiencing Psychological Distress: A Hermeneutic Single Case Efficacy Design (HSCED) Series
Actual Study Start Date :
Apr 29, 2020
Actual Primary Completion Date :
Nov 18, 2020
Actual Study Completion Date :
Dec 18, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Psychological therapy

All participants will receive psychological therapy. There will be no placebos or waiting list controlled participants to compare findings to.

Other: Psychological therapy
Acceptance and Commitment Therapy (ACT) is a trans-diagnostic approach which aims to promote better living by supporting clients through six key processes (e.g. mindfulness, values). ACT does not aim to reduce distress, rather its goal is to promote better living or a better quality of life despite distress (Hayes, Strosahl & Wilson, 1999). ACT has been shown to have equal or superior efficacy to CBT with a number of psychological and physical health conditions (A-Tjak et al., 2015; Ruiz, 2012).
Other Names:
  • Acceptance and Commitment Therapy
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Quality of Life Assessed Using the Older People's Quality of Life Questionnaire (OPQOL-brief; Bowling, Hankins, Windle, Bilotta, & Grant, 2013). [up to 20 weeks]

      Brief measure of quality of life (QoL) in older age.

    Secondary Outcome Measures

    1. Client's Level of Cognitive Functioning Assessed Using the Montreal Cognitive Assessment (MoCA; Nasreddine et al., 2005). [up to 5 weeks]

      A brief cognitive screening questionnaire which will be administered by the usual care team at the start of the study.

    2. Symptoms of Anxiety and Depression Assessed With the Hospital Anxiety and Depression Scale (HADS; Zigmond & Snaith, 1983). [up to 20 weeks]

      A brief measure of anxiety and depression that is less prone to conflation of physical health symptoms onto symptoms of psychological distress.

    3. Change in/Progress on Client's Goals Assessed Using the Simplified Personal Questionnaire (PQ; Elliot, Mack, & Shapiro, 1999). [up to 20 weeks]

      This consists of up to ten problem statements the client outlines at start of therapy and rates on a 7-point Likert scale for how much they have been bothered by the problem in the past week. They will then re-rate this before each therapy session and again at six-week follow-up.

    4. Change in Client's Weekly Level of Quality of Life Assessed Using the Outcome Rating Scale (ORS; Miller, Duncan, Brown, Sparks & Claud, 2003). [up to 20 weeks]

      A brief measure of patient rated outcomes in therapy session.

    5. Change in Therapeutic Alliance Assessed With the Session Rating Scale (SRS; Duncan et al., 2003). [up to 20 weeks]

      A brief measure of patient rated therapeutic alliance.

    6. Client's (Qualitative) Views on Individual Therapy Sessions Assessed With the Helpful Aspects of Therapy Form (HAT; Llewlyn et al., 1988). [up to 20 weeks]

      A qualitative measure of patient rated therapeutic alliance.

    7. Change in Psychological Flexibility Assessed Using the CompACT (Francis, Dawson, & Golijani-Moghaddam, 2016). [up to 20 weeks]

      An ACT process measure.

    8. Client's Attribution of Change and View on Therapy Assessed With the Change Interview (Elliott, Slatick, & Urman, 2001). [up to 20 weeks]

      A semi-structured interview to determine the participant's view on any change achieved during therapy. Delivered by a researcher other than the therapist.

    9. Adherence to ACT Related Processes Assessed With the ACT Fidelity Measure (ACT-FM; O'Neill, Latchford, McCracken & Graham, 2019). [up to 20 weeks]

      A fidelity measure to ensure that sessions meet the requirements of ACT.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Be at least 65 years of age.

    • Score at least 8 on the Hospital Anxiety and Depression Scale (HADS; ZIgmond & Snaith,

    1. on either the anxiety or depression sub-scale. The HADS is an outcome measure already used by the MHSOP.
    • Be referred to the MHSOP for psychological support.

    • Have capacity to give informed consent.

    • Be willing to engage in one-to-one psychotherapy.

    • Be able to travel to the service (either independently or with support).

    Exclusion Criteria:
    • A score lower than 22-24 on the MoCA. This is to screen for a level of cognitive deficit, which cannot be accommodated for in the current study, due to the adaptations which will be required (e.g. review sessions, carer enrolment to support memory consolidation). Cut-off limit is dependent on the individual's age and education history. The MoCA is administered by the MHSOP as standard practice.

    • Not rated higher than Cluster 8 (Mental Health Clustering Booklet 2013/14, Department of Health), a categorisation based on the Health of the Nation Outcome Scale (HoNOS; Wing et al., 1998). Clusters higher than 8 are associated with clients presenting with symptoms of psychosis and it is felt that this level of mental health problem would cause serious heterogeneity between client cases. As standard practice, the MHSOP at Ling Bar Hospital will have rated the client prior to consideration for the study.

    • Inability to understand English to a level required to participate fully in the intervention. This is due to a lack of ability to benefit from the intervention without an interpreter, and the impact an interpreter would have on the non-therapeutic processes (e.g. alliance) being measured in this study.

    • Not currently undertaking any other psychological therapy, talking therapy or counselling. This is due to the potential impact the other therapy could have on change and the inability to fully account for this.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mental Health Services for Older People Nottingham Nottinghamshire United Kingdom

    Sponsors and Collaborators

    • University of Lincoln

    Investigators

    • Principal Investigator: Nima Golijani-Moghaddam, Dr, University of Lincoln

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    University of Lincoln
    ClinicalTrials.gov Identifier:
    NCT04280445
    Other Study ID Numbers:
    • 191201
    First Posted:
    Feb 21, 2020
    Last Update Posted:
    Nov 2, 2021
    Last Verified:
    Jan 1, 2020
    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
    Keywords provided by University of Lincoln
    Additional relevant MeSH terms:

    Study Results

    Participant Flow

    Recruitment Details
    Pre-assignment Detail
    Arm/Group Title Psychological Therapy
    Arm/Group Description All participants will receive psychological therapy. There will be no placebos or waiting list controlled participants to compare findings to. Psychological therapy: Acceptance and Commitment Therapy (ACT) is a trans-diagnostic approach which aims to promote better living by supporting clients through six key processes (e.g. mindfulness, values). ACT does not aim to reduce distress, rather its goal is to promote better living or a better quality of life despite distress (Hayes, Strosahl & Wilson, 1999). ACT has been shown to have equal or superior efficacy to CBT with a number of psychological and physical health conditions (A-Tjak et al., 2015; Ruiz, 2012).
    Period Title: Overall Study
    STARTED 3
    COMPLETED 3
    NOT COMPLETED 0

    Baseline Characteristics

    Arm/Group Title Psychological Therapy
    Arm/Group Description All participants will receive psychological therapy. There will be no placebos or waiting list controlled participants to compare findings to. Psychological therapy: Acceptance and Commitment Therapy (ACT) is a trans-diagnostic approach which aims to promote better living by supporting clients through six key processes (e.g. mindfulness, values). ACT does not aim to reduce distress, rather its goal is to promote better living or a better quality of life despite distress (Hayes, Strosahl & Wilson, 1999). ACT has been shown to have equal or superior efficacy to CBT with a number of psychological and physical health conditions (A-Tjak et al., 2015; Ruiz, 2012).
    Overall Participants 3
    Age (Count of Participants)
    <=18 years
    0
    0%
    Between 18 and 65 years
    0
    0%
    >=65 years
    3
    100%
    Age (years) [Mean (Standard Deviation) ]
    Mean (Standard Deviation) [years]
    72.67
    (5.86)
    Sex: Female, Male (Count of Participants)
    Female
    2
    66.7%
    Male
    1
    33.3%
    Race/Ethnicity, Customized (Count of Participants)
    White British
    3
    100%
    Older People's Quality of Life questionnaire, brief version (OPQOL-brief; Bowling et al., 2013) (units on a scale) [Mean (Standard Deviation) ]
    Mean (Standard Deviation) [units on a scale]
    43.67
    (7.57)
    Hospital Anxiety and Depression Scale - Anxiety Subscale(HADS-A; Zigmond & Snaith, 1983) (units on a scale) [Mean (Standard Deviation) ]
    Mean (Standard Deviation) [units on a scale]
    13.67
    (6.66)
    Hospital Anxiety and Depression Scale - Depression Subscale (HADS-D; Zigmond & Snaith, 1983) (units on a scale) [Mean (Standard Deviation) ]
    Mean (Standard Deviation) [units on a scale]
    9.67
    (3.06)
    Comprehensive Assessment of Acceptance and Commitment Therapy processes, short-form,(CompACT-8; Morr (units on a scale) [Mean (Standard Deviation) ]
    Mean (Standard Deviation) [units on a scale]
    20
    (1.73)

    Outcome Measures

    1. Primary Outcome
    Title Change in Quality of Life Assessed Using the Older People's Quality of Life Questionnaire (OPQOL-brief; Bowling, Hankins, Windle, Bilotta, & Grant, 2013).
    Description Brief measure of quality of life (QoL) in older age.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    All participants completed baseline of 3 or 4 weeks. OPQOL-brief was used at baseline, mid, end, and follow-up point. Missing data was treated as missing. Mean score for all participants at one-month follow-up point shown below.
    Arm/Group Title Psychological Therapy
    Arm/Group Description All participants will receive psychological therapy. There will be no placebos or waiting list controlled participants to compare findings to. Psychological therapy: Acceptance and Commitment Therapy (ACT) is a trans-diagnostic approach which aims to promote better living by supporting clients through six key processes (e.g. mindfulness, values). ACT does not aim to reduce distress, rather its goal is to promote better living or a better quality of life despite distress (Hayes, Strosahl & Wilson, 1999). ACT has been shown to have equal or superior efficacy to CBT with a number of psychological and physical health conditions (A-Tjak et al., 2015; Ruiz, 2012).
    Measure Participants 3
    Mean (Standard Deviation) [score on a scale]
    43.33
    (8.39)
    2. Secondary Outcome
    Title Client's Level of Cognitive Functioning Assessed Using the Montreal Cognitive Assessment (MoCA; Nasreddine et al., 2005).
    Description A brief cognitive screening questionnaire which will be administered by the usual care team at the start of the study.
    Time Frame up to 5 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    3. Secondary Outcome
    Title Symptoms of Anxiety and Depression Assessed With the Hospital Anxiety and Depression Scale (HADS; Zigmond & Snaith, 1983).
    Description A brief measure of anxiety and depression that is less prone to conflation of physical health symptoms onto symptoms of psychological distress.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    4. Secondary Outcome
    Title Change in/Progress on Client's Goals Assessed Using the Simplified Personal Questionnaire (PQ; Elliot, Mack, & Shapiro, 1999).
    Description This consists of up to ten problem statements the client outlines at start of therapy and rates on a 7-point Likert scale for how much they have been bothered by the problem in the past week. They will then re-rate this before each therapy session and again at six-week follow-up.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    5. Secondary Outcome
    Title Change in Client's Weekly Level of Quality of Life Assessed Using the Outcome Rating Scale (ORS; Miller, Duncan, Brown, Sparks & Claud, 2003).
    Description A brief measure of patient rated outcomes in therapy session.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    6. Secondary Outcome
    Title Change in Therapeutic Alliance Assessed With the Session Rating Scale (SRS; Duncan et al., 2003).
    Description A brief measure of patient rated therapeutic alliance.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    7. Secondary Outcome
    Title Client's (Qualitative) Views on Individual Therapy Sessions Assessed With the Helpful Aspects of Therapy Form (HAT; Llewlyn et al., 1988).
    Description A qualitative measure of patient rated therapeutic alliance.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    8. Secondary Outcome
    Title Change in Psychological Flexibility Assessed Using the CompACT (Francis, Dawson, & Golijani-Moghaddam, 2016).
    Description An ACT process measure.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    9. Secondary Outcome
    Title Client's Attribution of Change and View on Therapy Assessed With the Change Interview (Elliott, Slatick, & Urman, 2001).
    Description A semi-structured interview to determine the participant's view on any change achieved during therapy. Delivered by a researcher other than the therapist.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description
    10. Secondary Outcome
    Title Adherence to ACT Related Processes Assessed With the ACT Fidelity Measure (ACT-FM; O'Neill, Latchford, McCracken & Graham, 2019).
    Description A fidelity measure to ensure that sessions meet the requirements of ACT.
    Time Frame up to 20 weeks

    Outcome Measure Data

    Analysis Population Description
    [Not Specified]
    Arm/Group Title
    Arm/Group Description

    Adverse Events

    Time Frame 6 months
    Adverse Event Reporting Description
    Arm/Group Title Psychological Therapy
    Arm/Group Description All participants will receive psychological therapy. There will be no placebos or waiting list controlled participants to compare findings to. Psychological therapy: Acceptance and Commitment Therapy (ACT) is a trans-diagnostic approach which aims to promote better living by supporting clients through six key processes (e.g. mindfulness, values). ACT does not aim to reduce distress, rather its goal is to promote better living or a better quality of life despite distress (Hayes, Strosahl & Wilson, 1999). ACT has been shown to have equal or superior efficacy to CBT with a number of psychological and physical health conditions (A-Tjak et al., 2015; Ruiz, 2012).
    All Cause Mortality
    Psychological Therapy
    Affected / at Risk (%) # Events
    Total 0/3 (0%)
    Serious Adverse Events
    Psychological Therapy
    Affected / at Risk (%) # Events
    Total 0/3 (0%)
    Other (Not Including Serious) Adverse Events
    Psychological Therapy
    Affected / at Risk (%) # Events
    Total 0/3 (0%)

    Limitations/Caveats

    [Not Specified]

    More Information

    Certain Agreements

    Principal Investigators are NOT employed by the organization sponsoring the study.

    There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

    Results Point of Contact

    Name/Title Dr Daniell De Boos
    Organization Trent Doctorate in Clinical Psychology Programme, University of Nottingham, UK
    Phone +44 (0)115 84 67523
    Email danielle.deboos@nottingham.ac.uk
    Responsible Party:
    University of Lincoln
    ClinicalTrials.gov Identifier:
    NCT04280445
    Other Study ID Numbers:
    • 191201
    First Posted:
    Feb 21, 2020
    Last Update Posted:
    Nov 2, 2021
    Last Verified:
    Jan 1, 2020