Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04015505
Other study ID # 248358
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 27, 2019
Est. completion date January 21, 2020

Study information

Verified date February 2020
Source University of East Anglia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to evaluate a specific psychological technique to help older adults with depression improve their mood and develop or utilise their 'wisdom' for managing their current difficulties. The United Kingdom (UK) population is ageing and effective psychological therapies for older adults need to be well evaluated and developed. This study aims to develop evidence for this technique, and links between gerontological theories of wisdom and clinical psychology.

The 'timeline' technique (Laidlaw, 2010, 2015) is recommended within Cognitive Behavioural Therapy (CBT) for older adults. CBT is the most evidenced based psychological treatment for a range of psychiatric disorders including depression. Outcome studies have found that older people are just as likely to respond to CBT as younger people.

This technique draws on theories of 'wisdom', where one's wisdom can develop from how they reflect on their life experiences. Depressed individuals may view their lives in overgeneralised negative ways, making this process harder. The timeline technique asks people to create a timeline of their lives. Through reflection and discussion of past events, they are helped to recognise personal resilience, develop self-compassion, and utilise their wisdom for managing current difficulties. This technique requires specific evaluation to determine its validity and effectiveness.

This study uses a single-case experimental research design to allow conclusions to be drawn from a small number of participants. Six individuals from primary and secondary care mental health waiting lists, as well as third sector providers, aged over 60 and experiencing depression or low mood, will be invited to take part in a short testing of this technique. Individuals will be asked to measure their mood and complete relevant questionnaires throughout their involvement in the study and will do this for up to 4 weeks on their own. They will then meet with a trainee clinical psychologist for five weekly sessions of a structured therapy using the timeline technique.


Description:

BACKGROUND

The United Kingdom (UK) population is getting older, with those over 65 predicted to reach 24% by 2037 (Office for National Statistics, 2017). With improved quality of life and advances in healthcare, there is increased pressure on services to cater for the wellbeing of older adults. UK government states that depression affects one in five older people living in the community (UK Government, 2017). Depression is therefore a significant mental health condition for older adults and for which effective treatments and approaches are required. As such, there is a growing need to tailor psychological therapies to the older adult population and for new techniques to be well evaluated.

'Cognitive behavioural therapy (CBT) for older adults' augments traditional evidence-based CBT for the older adult population with 'age-appropriate' techniques, developed from lifespan developmental models and gerontological theory to help enhance treatment outcomes for older adults (Knight & Laidlaw, 2009; Laidlaw, 2010). One technique is the 'wisdom enhancement' timeline technique (Laidlaw, 2010, 2015; Laidlaw & Kishita, 2015), which builds on a psychological model of wisdom applied to clinical psychology. The technique has roots in classical cognitive behavioural techniques but is distinctive in how it uses one's life narrative as a resource. The timeline technique can be regarded as an innovative and structured way of using peoples' life narratives and experiences in a cognitive-behavioural framework to evolve the psychological resource of wisdom and increase mood and coping in the present. It is time-limited and present problem focused. The timeline technique is recommended in Increased Access to Psychological Therapies Services (IAPT) guidelines for CBT for older adults, meaning that it will be routinely used in National Health Service (NHS) settings in England. The timeline technique is theorised to improve mood by increasing self-acceptance and wisdom. However, the technique has not been specifically tested in detail.

PURPOSE OF THE STUDY

This study will investigate in detail the 'wisdom enhancement' timeline technique for helping older adults with depression develop 'wisdom', self-compassion and improve mood. The study will use a single-case experimental design to evaluate the technique's effectiveness and mechanisms of change. It will provide a valuable examination of a specific recommended CBT technique, where there is a general need for more testing of individual components of therapy. The results from this investigation will help inform further developments of wisdom enhancement models in clinical psychology and efficacy of CBT for older adults.

RESEARCH AIM

The primary aim of this study is to evaluate the 'timeline technique' (Laidlaw, 2015) with older adults experiencing mild-moderate depression. This will be achieved by delivering a short psychological intervention to older adults using the timeline technique, based on appropriate guidelines. Principle research questions:

1. Does the timeline intervention reduce negative affect?

2. Does the timeline intervention increase self-compassion?

3. Does the timeline intervention increase wisdom for managing current difficulties?

STUDY DESIGN

This study uses a single case experimental design (SCED) to measure the effects that the 'timeline' intervention has on mood, self-compassion and wisdom, as measured by structured self-report questionnaires and idiographic measures. Older adults experiencing depression/low mood will be recruited from NHS primary and secondary care or third sector psychological treatment waiting lists.

SCEDs have long been used in psychology intervention research and are a useful method for examining the effectiveness of an intervention on individuals with only a few participants (Morgan & Morgan, 2001; Kazdin, 2011). Unlike randomised controlled trials, each participant acts as their own control by measuring their baseline state for a period of time before the intervention is introduced. Each participant will take part in three phases:

1. Baseline phase: participants will complete weekly standardised measures of mood and daily idiographic measures of mood, self-compassion and wisdom.

2. Intervention phase: participants will receive a 5 week psychological intervention, whilst continuing to complete the baseline measures. This will allow for any observable change in mood during the onset of the intervention to be determined.

3. Participants will complete a single set of follow up measures 1 month after the intervention phase ends.

Participants will also complete standardised measures of mood, self-compassion and wisdom at pre-baseline, pre-intervention and post-intervention time points, to allow for further between phase testing. Measurement during the intervention phase and at follow up will account for effects of the intervention that accrue slowly over time and test if any effects are sustained.

The study adopts an across-participant multiple baseline component which means that each participant will be randomly assigned to one of three pre-determined baseline phases of differing lengths:

Group A: 2 weeks Group B: 3 weeks Group C: 4 weeks The multiple baseline design is the most frequent design used in psychology single case studies (Smith, 2012) and allows for greater control for determining when changes in the target variable are attributed to a specific study phase.

Participants will take part once they are recruited and it is convenient for them to take part, rather than needing to all start simultaneously. This is therefore considered a non-concurrent multiple baseline design and allows greater flexibility for both researchers and participants.

ADDITIONAL INFO

This study is taking place as part of the chief investigator's research training and qualification for a UK Doctorate in Clinical Psychology.


Recruitment information / eligibility

Status Completed
Enrollment 7
Est. completion date January 21, 2020
Est. primary completion date January 21, 2020
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Adults aged over 60.

- Primary problem depression, as measured by the screening tool PHQ-9 cut off point of 5.

- Currently on a waiting list for psychological treatment or considered treatment resistant.

- Low risk for suicide or self-harm, as screened through recruiting clinicians, health records and clinical judgement of the researcher

- Absence of cognitive impairment or substance misuse

- Participants should be on a stable dose, at least 3 months without change, of antidepressant medication

- Able to speak and understand English

Exclusion Criteria:

- Must not already be receiving any active psychological treatment for depression, or changes to any antidepressant medication in the past three months. If participants are on antidepressant medication which has not been changed in the last three months they will be still be eligible - this will be considered a stable dose.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Behavioural Therapy for older adults: wisdom enhancement 'timeline technique'
The intervention is comprised of five one-hour sessions of structured talking therapy, where participants create a timeline of their life with significant events included. Through dialogue with the therapist and structured worksheets, participants are encouraged to reflect on events in their life to recognise and develop qualities of resilience and self-compassion. They are then asked to use 'the wisdom of their years' to develop strategies to manage difficulties they are currently facing. Participants will also be asked to complete worksheets and try out new strategies between sessions.

Locations

Country Name City State
United Kingdom Cambridge and Peterborough NHS Foundation Trust Cambridge
United Kingdom Norfolk and Suffolk NHS Foundation Trust Norwich

Sponsors (1)

Lead Sponsor Collaborator
University of East Anglia

Country where clinical trial is conducted

United Kingdom, 

References & Publications (15)

Elliott R. Hermeneutic single-case efficacy design. Psychother Res. 2002 Mar 1;12(1):1-21. doi: 10.1080/713869614. — View Citation

Kazdin, AE. Single-case research designs: Methods for clinical and applied settings. Oxford University Press, 2011.

Knight BG, Laidlaw, K. Translational theory: A wisdom-based model for psychological interventions to enhance well-being in later life. In V. L. Bengston, D. Gans, N. M. Pulney, & M. Silverstein (Eds.), Handbook of theories of aging (pp. 693-705). New York, NY, US: Springer Publishing Co. 2009.

Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001 Sep;16(9):606-13. — View Citation

Laidlaw K, Kishita, N. Age-appropriate augmented cognitive behavior therapy to enhance treatment outcome for late-life depression and anxiety disorders. Geropsych 28: 57-66, 2015.

Laidlaw K. Are attitudes to ageing and wisdom enhancement legitimate targets for CBT for late life depression and anxiety?. Nordic Psychology 62: 27-42, 2010.

Laidlaw K. CBT for older people: An introduction. Sage, London, 2015.

Laidlaw K. Enhancing cognitive behavior therapy with older people using gerontological theories as vehicles for change. Casebook of Clinical Geropsychology: International Perspectives on Practice, 17, 2010.

Morgan DL, Morgan RK. Single-participant research design. Bringing science to managed care. Am Psychol. 2001 Feb;56(2):119-27. Review. — View Citation

Mueller AE, Segal DL, Gavett B, Marty MA, Yochim B, June A, Coolidge FL. Geriatric Anxiety Scale: item response theory analysis, differential item functioning, and creation of a ten-item short form (GAS-10). Int Psychogeriatr. 2015 Jul;27(7):1099-111. doi: 10.1017/S1041610214000210. Epub 2014 Feb 27. — View Citation

Neff KD. The development and validation of a scale to measure self-compassion. Self and identity 2(3): 223-250, 2003.

Office for National Statistics (2017). Overview of the UK population: July 2017. Retrieved from https://www.ons.gov.uk/peoplepopulationandcommunity/populationandmigration/populationestimates/articles/overviewoftheukpopulation/july2017

Smith JD. Single-case experimental designs: a systematic review of published research and current standards. Psychol Methods. 2012 Dec;17(4):510-50. doi: 10.1037/a0029312. Epub 2012 Jul 30. Review. — View Citation

UK Government (2017) Living Well in Older Years. Retrieved from: https://www.gov.uk/government/publications/better-mental-health-jsna-toolkit/7-living-well-in-older-years#fn:4

Webster JD. Measuring the character strength of wisdom. Int J Aging Hum Dev. 2007;65(2):163-83. — View Citation

* Note: There are 15 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Other Change interview questionnaire (non standardised brief qualitative questionnaire) The 'Change interview questionnaire' is a three question qualitative questionnaire that has been created by the research team to be used specifically for this study. It is therefore not a standardised measure or scale.
The questionnaire comprises of three qualitative questions based on the key information elicited in the semi-structured 'Change Interview' (Elliot, 2002), adapted to the format of a written questionnaire.
This questionnaire asks the following three questions:
What has changed for you over the course of the study?
Why do you think these changes occurred?
What has been helpful?
Participants are asked to write qualitative answers to each question using the free space provided after each question.
The answers to these questions will not be included in any formal analysis but will provide additional information in helping to evaluate the validity of any intervention effects for each case.
Group A: At week 7 / End of intervention period
Other Change interview questionnaire (non standardised brief qualitative questionnaire) The 'Change interview questionnaire' is a three question qualitative questionnaire that has been created by the research team to be used specifically for this study. It is therefore not a standardised measure or scale.
The questionnaire comprises of three qualitative questions based on the key information elicited in the semi-structured 'Change Interview' (Elliot, 2002), adapted to the format of a written questionnaire.
This questionnaire asks the following three questions:
What has changed for you over the course of the study?
Why do you think these changes occurred?
What has been helpful?
Participants are asked to write qualitative answers to each question using the free space provided after each question.
The answers to these questions will not be included in any formal analysis but will provide additional information in helping to evaluate the validity of any intervention effects for each case.
Group B: At week 8 / End of intervention period
Other Change interview questionnaire (non standardised brief qualitative questionnaire) The 'Change interview questionnaire' is a three question qualitative questionnaire that has been created by the research team to be used specifically for this study. It is therefore not a standardised measure or scale.
The questionnaire comprises of three qualitative questions based on the key information elicited in the semi-structured 'Change Interview' (Elliot, 2002), adapted to the format of a written questionnaire.
This questionnaire asks the following three questions:
What has changed for you over the course of the study?
Why do you think these changes occurred?
What has been helpful?
Participants are asked to write qualitative answers to each question using the free space provided after each question.
The answers to these questions will not be included in any formal analysis but will provide additional information in helping to evaluate the validity of any intervention effects for each case.
Group C: At week 9 / End of intervention period
Primary 9-item Patient Health Questionnaire - assessing levels of change over time for each participant 9 item self-report measure for depression. (PHQ-9; Kroenke, Spitzer, & Williams, 2001).
The PHQ-9 is a brief and widely used nine-item self-report tool for measuring depression. Total scores range from 0 to 27 with higher scores suggesting higher severity of depression. This measure will be used as a primary outcome measure to monitor changes in mood across the duration of the study and will be assessed each week. The PHQ-9 will also be used as a study screening tool with a score above 5 (indicating mild depression; Kroenke et al., 2001) set as the cut-off point.
Group A: Weekly throughout study completion, up to 7 weeks and once at 1 month follow-up: at week 11
Primary 9-item Patient Health Questionnaire - assessing levels of change over time for each participant 9 item self-report measure for depression. (PHQ-9; Kroenke, Spitzer, & Williams, 2001).
The PHQ-9 is a brief and widely used nine-item self-report tool for measuring depression. Total scores range from 0 to 27 with higher scores suggesting higher severity of depression. This measure will be used as a primary outcome measure to monitor changes in mood across the duration of the study and will be assessed each week. The PHQ-9 will also be used as a study screening tool with a score above 5 (indicating mild depression; Kroenke et al., 2001) set as the cut-off point.
Group B: Weekly throughout study completion, up to 8 weeks and once at 1 month follow-up: at week 12
Primary 9-item Patient Health Questionnaire - assessing levels of change over time for each participant 9 item self-report measure for depression. (PHQ-9; Kroenke, Spitzer, & Williams, 2001).
The PHQ-9 is a brief and widely used nine-item self-report tool for measuring depression. Total scores range from 0 to 27 with higher scores suggesting higher severity of depression. This measure will be used as a primary outcome measure to monitor changes in mood across the duration of the study and will be assessed each week. The PHQ-9 will also be used as a study screening tool with a score above 5 (indicating mild depression; Kroenke et al., 2001) set as the cut-off point.
Group C: Weekly throughout study completion, up to 9 weeks and once at 1 month follow-up: at week 13
Primary 10-item Geriatric Anxiety Scale - assessing levels of change over time for each participant 10 item self-report measure for anxiety in later life. (GAS-10; Mueller et al, 2015).
The GAS-10 is a brief 10 item scale is a shorty form scale adapted from the 30-item Geriatric Anxiety Scale (Segal, June, Payne, Coolidge, & Yochim, 2010). It is a self-report questionnaire designed to measure severity of anxiety for older adults. Total scores range from 0 to 30, with higher total scores meaning higher levels of anxiety.
Group A: Weekly throughout study completion, up to 7 weeks and once at 1 month follow-up: at week 11
Primary 10-item Geriatric Anxiety Scale - assessing levels of change over time for each participant 10 item self-report measure for anxiety in later life. (GAS-10; Mueller et al, 2015).
The GAS-10 is a brief 10 item scale is a shorty form scale adapted from the 30-item Geriatric Anxiety Scale (Segal, June, Payne, Coolidge, & Yochim, 2010). It is a self-report questionnaire designed to measure severity of anxiety for older adults. Total scores range from 0 to 30, with higher total scores meaning higher levels of anxiety.
Group B: Weekly throughout study completion, up to 8 weeks and once at 1 month follow-up: at week 12
Primary 10-item Geriatric Anxiety Scale - assessing levels of change over time for each participant 10 item self-report measure for anxiety in later life. (GAS-10; Mueller et al, 2015).
The GAS-10 is a brief 10 item scale is a shorty form scale adapted from the 30-item Geriatric Anxiety Scale (Segal, June, Payne, Coolidge, & Yochim, 2010). It is a self-report questionnaire designed to measure severity of anxiety for older adults. Total scores range from 0 to 30, with higher total scores meaning higher levels of anxiety.
Group C: Weekly throughout study completion, up to 9 weeks and once at 1 month follow-up: at week 13
Primary Idiographic visual analogue scale - assessing daily change over time for each participant Self-reported idiographic visual analogue scale with specific questions developed in accordance with the study hypotheses:
Today, I feel that my mood is good
Today, I feel accepting of myself
Today, I feel that I can use the wisdom of my life to help deal with current difficulties
Idiographic measures are often used as well as standardized measures in single case design. They allow for specific target constructs to be measured in a way that is repeatable and efficient. The visual analogue scale consists of a ten-centimeter line anchored at either end with maximal and minimal extremes of the dimension being measured. Participants put a mark on the line, with the mark closer to the right side indicating stronger agreement of that statement. A numerical measurement of the line gives a score for each statement based on length (between 0 and 10.)
Group A: Daily through study completion, for total of 43 days and once at 1 month following end of intervention period: at week 11
Primary Idiographic visual analogue scale - assessing daily change over time for each participant Self-reported idiographic visual analogue scale with specific questions developed in accordance with the study hypotheses:
Today, I feel that my mood is good
Today, I feel accepting of myself
Today, I feel that I can use the wisdom of my life to help deal with current difficulties
Idiographic measures are often used as well as standardized measures in single case design. They allow for specific target constructs to be measured in a way that is repeatable and efficient. The visual analogue scale consists of a ten-centimeter line anchored at either end with maximal and minimal extremes of the dimension being measured. Participants put a mark on the line, with the mark closer to the right side indicating stronger agreement of that statement. A numerical measurement of the line gives a score for each statement based on length (between 0 and 10.)
Group B: Daily through study completion, for total of 50 days and once at 1 month following end of intervention period: at week 12
Primary Idiographic visual analogue scale - assessing daily change over time for each participant Self-reported idiographic visual analogue scale with specific questions developed in accordance with the study hypotheses:
Today, I feel that my mood is good
Today, I feel accepting of myself
Today, I feel that I can use the wisdom of my life to help deal with current difficulties
Idiographic measures are often used as well as standardized measures in single case design. They allow for specific target constructs to be measured in a way that is repeatable and efficient. The visual analogue scale consists of a ten-centimeter line anchored at either end with maximal and minimal extremes of the dimension being measured. Participants put a mark on the line, with the mark closer to the right side indicating stronger agreement of that statement. A numerical measurement of the line gives a score for each statement based on length (between 0 and 10.)
Group C: Daily through study completion, for total of 57 days and once at 1 month following end of intervention period: at week 13
Primary Self-compassion scale - assessing levels of change over time for each participant 26-item self-report measure of self-compassion (SCS; Neff, 2003)
26-item self-report measure of self-compassion measures overall self-compassion as well as six subscales, representing components of self-compassion: self-kindness versus self-judgment, sense of common humanity versus isolation, and mindfulness versus over-identification. Responses to each question are given on a 5-point Likert scale, from 'almost never' to 'almost always'. Subscale scores are computed by calculating the mean of subscale item responses, and therefore range from 0-5 with higher scores indicating higher levels of that construct. Total self-compassion score is calculated by reverse scoring the negative subscale items before calculating subscale means - self-judgment, isolation, and over-identification, then calculating a grand mean of all six subscale means. The total score ranges from 0-5 with higher scores indicating higher levels overall self-compassion.
Group A: At week 1, week 3, week 7, week 11.
Primary Self-compassion scale - assessing levels of change over time for each participant 26-item self-report measure of self-compassion (SCS; Neff, 2003)
26-item self-report measure of self-compassion measures overall self-compassion as well as six subscales, representing components of self-compassion: self-kindness versus self-judgment, sense of common humanity versus isolation, and mindfulness versus over-identification. Responses to each question are given on a 5-point Likert scale, from 'almost never' to 'almost always'. Subscale scores are computed by calculating the mean of subscale item responses, and therefore range from 0-5 with higher scores indicating higher levels of that construct. Total self-compassion score is calculated by reverse scoring the negative subscale items before calculating subscale means - self-judgment, isolation, and over-identification, then calculating a grand mean of all six subscale means. The total score ranges from 0-5 with higher scores indicating higher levels overall self-compassion.
Group B: At week 1, week 4, week 8, week 12.
Primary Self-compassion scale - assessing levels of change over time for each participant 26-item self-report measure of self-compassion (SCS; Neff, 2003)
26-item self-report measure of self-compassion measures overall self-compassion as well as six subscales, representing components of self-compassion: self-kindness versus self-judgment, sense of common humanity versus isolation, and mindfulness versus over-identification. Responses to each question are given on a 5-point Likert scale, from 'almost never' to 'almost always'. Subscale scores are computed by calculating the mean of subscale item responses, and therefore range from 0-5 with higher scores indicating higher levels of that construct. Total self-compassion score is calculated by reverse scoring the negative subscale items before calculating subscale means - self-judgment, isolation, and over-identification, then calculating a grand mean of all six subscale means. The total score ranges from 0-5 with higher scores indicating higher levels overall self-compassion.
Group C: At week 1, week 5, week, 9, week 13
Primary Self-Assessed Wisdom Scale (SAWS) - assessing levels of change over time for each participant 40-item self-report measure of wisdom (SAWS; Webster, 2007)
This 40-item self-report measure of wisdom uses a 6-point Likert scale to measure five subscales of wisdom: critical life experience, reminiscence and reflectiveness, openness, emotional regulation, and humor.
Each subsale total ranges from 0 to 40, with higher numbers indicating higher levels of that construct.
Adding total subscale scores together will generate a total SAWS wisdom score, with values ranging from 40 to 200, with a higher score indicating an overall higher level of wisdom.
Group A: At week 1, week 3, week 7, week 11.
Primary Self-Assessed Wisdom Scale (SAWS) - assessing levels of change over time for each participant 40-item self-report measure of wisdom (SAWS; Webster, 2007)
This 40-item self-report measure of wisdom uses a 6-point Likert scale to measure five subscales of wisdom: critical life experience, reminiscence and reflectiveness, openness, emotional regulation, and humor.
Each subsale total ranges from 0 to 40, with higher numbers indicating higher levels of that construct.
Adding total subscale scores together will generate a total SAWS wisdom score, with values ranging from 40 to 200, with a higher score indicating an overall higher level of wisdom.
Group B: At week 1, week 4, week 8, week 12.
Primary Self-Assessed Wisdom Scale (SAWS) - assessing levels of change over time for each participant 40-item self-report measure of wisdom (SAWS; Webster, 2007)
This 40-item self-report measure of wisdom uses a 6-point Likert scale to measure five subscales of wisdom: critical life experience, reminiscence and reflectiveness, openness, emotional regulation, and humor.
Each subsale total ranges from 0 to 40, with higher numbers indicating higher levels of that construct.
Adding total subscale scores together will generate a total SAWS wisdom score, with values ranging from 40 to 200, with a higher score indicating an overall higher level of wisdom.
Group C: At week 1, week 5, week, 9, week 13
See also
  Status Clinical Trial Phase
Completed NCT04289298 - Reaching and Engaging Depressed Senior Center Clients N/A
Not yet recruiting NCT06042283 - Efficacy of Metacognitive Training in Older Adults With Depression N/A
Completed NCT04078282 - The Use of Collaborative Care in General Practice for Elderly Patients With Depression N/A
Withdrawn NCT04055155 - Technology-enabled Task-sharing for Depression in Primary Care
Recruiting NCT06270121 - Development of a Healthcare Service Platform for Successful Aging N/A
Recruiting NCT05611996 - PEERS Plus mHealth Enhanced Peer Support N/A
Completed NCT04979299 - Assessment of Depression (iCGI) in Older People, According to Their Presentation in a Wheelchair or an Ordinary Chair. N/A
Completed NCT04404621 - Computer Presented and Physical Exercises to Maintain Cognitive Function and Emotional Health in Older Adults N/A
Not yet recruiting NCT06358404 - Developing a Peer Support Intervention for Depression in SCD N/A
Recruiting NCT06107283 - Study of the Reduction of the Prescriptions of Benzodiazepines and Related
Enrolling by invitation NCT04747756 - Creating a Virtual Village for People Aging With HIV During COVID-19 N/A
Completed NCT05308082 - Programme Evaluation on Effectiveness of The Use of Movement-based x 'Elderspirituality - Fu Le Mun Sum' Intervention to Support Elderly People With Depressive Symptoms N/A
Recruiting NCT05356611 - Engage for Late-Life Depression and Comorbid Executive Dysfunction N/A
Recruiting NCT03304301 - Effect of Sunlight Exposure and Outdoor Activities on Depression, Cognition and Quality of Life in the Elderly N/A
Recruiting NCT05967390 - Localized Analysis of Normalized Distance From Scalp to Cortex and Personalized Evaluation (LANDSCAPE)
Recruiting NCT05331599 - Recurrence Markers, Cognitive Burden and Neurobiological Homeostasis in Late-Life Depression
Completed NCT04258579 - Trial to Test Effectiveness of Depression Intervention for Mistreated Older Adults N/A
Withdrawn NCT04836533 - Enhancing Processing Speed and Executive Functioning in Depressed Older Adults With Computerized Cognitive Training Phase 1
Recruiting NCT05739370 - Internet Delivered Psychotherapy for Older Adults N/A
Recruiting NCT03256760 - Sleep and Healthy Aging Research for Depression (SHARE-D) Study Phase 1