CClinicalTrials.gg
CompletedNCT04552717Updated May 11, 2023

My Grief - an App for Parents With Prolonged Grief After Losing a Child to Cancer

An interventional study of My Grief in Prolonged Grief Disorder, sponsored by Uppsala University. Completed at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-05-11.

Sponsored by Uppsala University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
248
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Bereaved parents are at increased risk of developing mental and physical health problems and bereavement is even associated with an increased risk of mortality, especially in mothers. Prolonged grief disorder (PGD) are persistent and intensive grief reactions which can persist for years. It is characterized by an intense and lasting yearning for the deceased, intense emotional pain, such as difficulty accepting the loss and an inability to experience positive mood. Parents are among the most vulnerable to develop PGD.

The goal is to increase the accessibility to evidence-based and cost-effective interventions for parents of children who have died of cancer, and thus facilitate the grieving process and decrease the risk for parents to develop long-term distress.

Specific aims are:

  • To evaluate the acceptability and feasibility of a mobile app, "My Grief ", a self-help app for prolonged grief, in parents who lost a child to cancer.
  • To evaluate possible beneficial effects of the mobile app on parents' mental health.
Read the detailed description

There is a lack of studies evaluating the effect of interventions for bereaved parents. Thus, there is a need for accessible interventions with documented efficacy for preventing or reducing negative mental health consequences after the loss of a child. Today, many individuals carry smartphones and these devices can be used to access self-help interventions aiming to improve both physical and mental health. Currently, there are an excess of apps available for smartphone users that assert that they help people with their physical or mental health. However, for most of these apps, there is a lack of empirical support, i.e., their efficacy is unknown. It is therefore important to evaluate mobile apps in scientific studies with rigorous designs. In addition, before conducting rigorous studies of novel psychosocial interventions, such as a mobile app, it is important to conduct more basic work evaluating development and feasibility of the intervention. One such self-help app, the PTSD Coach, has been evaluated in a randomized controlled trial conducted with traumatized participants recruited from the community, which found that access to the PTSD Coach app was associated with improvements in posttraumatic stress (PTS) symptoms, depression, and psychosocial functioning. The PTSD Coach app is based on cognitive behavioural therapy (CBT) principles and there is a growing body of evidence that elements of CBT are effective interventions for prolonged grief. Thus, an app targeting prolonged grief using elements of CBT could potentially be effective in improving the mental health in bereaved parents. To our knowledge no such app has been developed and evaluated. The Grief Coach app will be based on the smartphone app PTSD Coach. A Swedish version of the PTSD Coach has been developed and a pilot study has been conducted as well as an ongoing RCT. Consultant programmers at Uppsala University will develop the mobile app. The content of the app will be developed together with experts in the field of grief, inspired by other grief apps and CBT therapy manuals, to modify parts of the PTSD Coach app to grief.

The main aim of this study is to examine the effectiveness of the app My Grief as compared to a waiting list comparison in reducing symptoms of prolonged grief in bereaved parents. The primary hypothesis is that the parents in the intervention group will report decreased levels of prolonged grief symptoms after having used the app. A second aim is to examine the effect of the app on related mental health problems (posttraumatic stress symptoms, depression symptoms, quality of life) and cognitive behavioral variables putatively explaining the effect of CBT techniques (i.e., grief avoidance, grief rumination and negative grief cognitions). The secondary hypotheses are that the parents in the intervention group will report improved mental health (i.e., lower symptom levels of depression and posttraumatic stress, higher quality of life), and lower grief avoidance, grief rumination, negative grief-related cognitions. A third aim is to evaluate the feasibility of the app, including participant satisfaction, evaluation of the app's strengths and weaknesses, and adverse events.

Potential participants are identified using the Swedish Childhood Cancer Registry, the Cause of Death Registry, and the Swedish Population Register at the Swedish Tax Agency. By linking the Cause of Death Registry with the Swedish Childhood Cancer Registry, children diagnosed with a malignancy and who died due to the malignancy 1 to 10 years previously will be identified. Next, the children's parents/caregivers are identified through the Swedish Population Register and will be sent a letter with an invitation to participate in the study. Participants will complete a web based pre-assessment and then given access to the app for three months followed by a web based post-assessment and an interview via telephone regarding their experiences of using the app, with follow-ups att 6 and 12 months.

02

Conditions studied

  • Prolonged Grief Disorder
03

In context

Prolonged Grief Disorder

39 studies on the registry are indexed under Prolonged Grief Disorder; 14 are open to participants now.

This study's enrollment of 248 is above the median of 68 across 35 interventional studies indexed under Prolonged Grief Disorder.

Browse Prolonged Grief Disorder studies →

Lead sponsor

Uppsala University is the lead sponsor of 381 studies on the registry; 84 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Parents/caregivers of children who have died of cancer, at the earliest 12 month ago
  • Have symptoms of prolonged grief (PGD)
  • Understand Swedish language
  • Have access to a smartphone

Exclusion criteria

Exclusion Criteria:

  • Ongoing severe psychiatric problems (e.g. suicidal thoughts, psychosis)
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
248 participants (actual)

Study arms

  • Experimental
    Intervention

    Participants will complete a web based pre-assessment and then given access to the app "My Grief" for three months followed by a web based post-assessment and an interview via telephone regarding their experiences of using the app, and follow-up questionnaires.

    Other: My Grief

  • No intervention
    Waitlist controll

    Participants will get access to the app after three months.

Interventions

  • OtherMy Grief

    The app will build on principles of cognitive behavioural theory and therapy (CBT) and contains four main sections: Learning, Self-assessment, Manage symptoms and Find support.

06

What researchers measure

Primary outcomes

  1. Change (from baseline) in Prolonged Grief Disorder-13 instrument, PG-13

    13-item, self-rated measure of prolonged grief, total score ranges from 11 to 55, where a higher score indicates more symptoms

    Time frame: 3, 6 and 12 months

Secondary outcomes

  1. Change (from baseline) in Posttraumatic stress disorder checklist for DSM-5, PCL-5

    20-item, self-rated measure of posttraumatic stress disorder, total score range from 0-80, and a higher score indicates more symptoms

    Time frame: 3, 6 and 12 months

  2. Change (from baseline) in Patient Health Questionnaire, PHQ-9

    9-item, self-rated measure of depression, total score ranges from 0-27, and a higher score indicates more symptoms

    Time frame: 3, 6 and 12 months

  3. Change (from baseline) in Utrecht Grief Rumination Scale, UGRS

    15-item, self-rated measure of grief rumination, total scores range from 15 to 75, and a higher score indicates more grief rumination

    Time frame: 3, 6 and 12 months

  4. Change (from baseline) in Depressive and Anxious Avoidance in Prolonged Grief questionnaire

    9-item, self-rated measure of avoidance, total score ranges from 9-72, and a higher score indicates more avoidance

    Time frame: 3, 6 and 12 months

  5. Change (from baseline) in 18 items from the Grief Cognitions Questionniare, GCQ

    18-items, self-rated measure of grief cognitions, total score ranges from 0-90, and a higher score indicates more grief cognitions

    Time frame: 3, 6 and 12 months

  6. Change (from baseline) in Brunnsviken Brief Quality of Life Inventory, BBQ

    12 items, self-rated measure of quality of life, covering six different life domains, Total score ranges from 0-96, higher scores indicates higher quality of life.

    Time frame: 3, 6 and 12 months

Other outcomes

  1. Feasibility of the intervention and the application

    Feasibility will be measured by "App Survey"

    Time frame: 3 months

  2. Acceptability of the intervention and the application

    Acceptability will be measured by "App Survey"

    Time frame: 3 months

  3. Participants demographics

    age, gender, time since loss, gender child, marital status, employment status, loss-related variables

    Time frame: 0 months

07

Study locations

1 site
  • National Centre for Disaster Psychiatry, Department of Neuroscience, Uppsala university
    Uppsala, 75185, Sweden
08

References and documents

Publications

  • Eklund R, Eisma MC, Boelen PA, Arnberg FK, Sveen J. My Grief App for Prolonged Grief in Bereaved Parents: A Pilot Study. Front Psychiatry. 2022 Apr 25;13:872314. doi: 10.3389/fpsyt.2022.872314. eCollection 2022. PubMed 35546953 ↗
  • Eklund R, Eisma MC, Boelen PA, Arnberg FK, Sveen J. Mobile app for prolonged grief among bereaved parents: study protocol for a randomised controlled trial. BMJ Open. 2021 Dec 7;11(12):e052763. doi: 10.1136/bmjopen-2021-052763. PubMed 34876429 ↗

Individual participant data

Plan to share: Yes — All collected IPD

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 11, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04552717
Lead sponsor
Uppsala University
Responsible party
Josefin Sveen (PhD, Uppsala University) — Principal investigator
First posted
Sep 17, 2020
Start date
Sep 15, 2021
Primary completion
Dec 31, 2022
Completion
May 8, 2023
Last update
May 11, 2023

Study contacts

Josefin Sveen, PhD
principal investigator · Uppsala University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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