PeriGrief: Walk With Me for Perinatal Grief

Sponsor
Oregon Research Behavioral Intervention Strategies, Inc. (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05318287
Collaborator
(none)
92
1
1
3.6
25.7

Study Details

Study Description

Brief Summary

This research will contribute to therapeutic technology to support bereaved parents who have experienced a perinatal loss. The proposed mobile application would accomplish this objective by providing a series of therapeutic modules to provide parents with tools to normalize their grief and additional coping skills to support the grieving process.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Walk with Me
N/A

Detailed Description

The investigators will develop grief processing and healing activities for bereaved parents, via an iterative formative development process with stakeholder input. The investigators will embed the core intervention components in administrative, provider, and client interfaces which will comprise the prototype Walk with Me (WWM) intervention.

The investigators will evaluate its feasibility and initial efficacy of WWM in a within-subjects pre-post design study. The investigators will provide the mobile-based provider component for use by HCPs who work in the partner hospital. HCPs will have access to training videos and bereaved parent content. After training, the HCPs will recruit 52 bereaved parents.

HCPs will obtain consent from bereaved parents who express interest in the study to share their contact information with the research team. Parents who wish to participate will provide consent for their own participation in the study. After consent, parents will complete the baseline survey via the Qualtrics online assessment form and then be provided download access to the WWM prototype. At 4 and 8 weeks, parents will be administered post-treatment surveys. This design will allow the investigators to evaluate baseline to follow-up change in the proposed study outcomes and acceptability of the prototype WWM program.

Baseline and post-treatment surveys will measure bereaved parents traumatic stress, grief intensity, grief, grief management self-efficacy, and care experiences. The post-survey questionnaire will contain measures of usability, as well as any difficulties experienced or problems made worse. Demographics will be collected at the baseline assessment. Project staff will follow-up with parents as needed to encourage survey completion in a timely manner.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
92 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Walk With Me (WWM) for Perinatal Grief
Anticipated Study Start Date :
Jul 15, 2022
Anticipated Primary Completion Date :
Sep 15, 2022
Anticipated Study Completion Date :
Nov 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: PeriGrief

A brief four-module intervention delivered via computer or mobile device. Modules utilize mindfulness and cognitive behavioral therapy strategies to reduce distress following perinatal loss.

Behavioral: Walk with Me
Walk with Me is a perinatal grief mobile application to provide supportive care to bereaved parents. The application includes modules to guide bereaved parents through strategies to help support them through their grieving.

Outcome Measures

Primary Outcome Measures

  1. Traumatic stress will be analyzed as change over time [Baseline (immediately following loss), 4 weeks and 8 weeks post loss]

    Impact of Event Scale-Revised includes 22 items on the past 7 days that represent symptoms of distress self-rated on a five-point scale: 0 indicates that the symptom occurs "not at all"; 1, "a little bit"; 2, "moderately"; 3, "quite a bit"; and 4, "extremely." Higher scores indicate greater distress/trauma. Participants will be instructed to relate the IES-R items specifically to the loss of their child. The investigators will examine scores as a continuous variable and presence/absence of diagnosis using a cutoff score of 35 or more.

  2. Grief intensity will be analyzed as change over time [Baseline (immediately following loss), 4 weeks and 8 weeks post loss]

    The Perinatal Grief Intensity Scale is 14 items that asks about an individuals' experiences with perinatal loss. Items are on a four-point scale (1 to 4) and is averaged across three scales with a total possible score of 4. Higher overall scores indicating higher intensity of grief.

  3. Grief [Baseline (immediately following loss)]

    The Perinatal Bereavement Scale is a 15-item scale designed as a measure of grief and yearning for the lost pregnancy and the lost baby. Respondents indicate how often the statement has been true in the past week, using a 4-point Likert-type scale ranging from rarely or none of the time, less than 1 day (scored 1) to most or all of the time, 5 to 7 days (scored 4). Responses are summed to yield a total score (possible range, 15-60)

  4. Grief management self-efficacy will be analyzed as a change over time [4 weeks and 8 weeks post loss]

    Three items that rate the bereaved parents' confidence in their ability to cope with grief, use knowledge of mindfulness skills to cope, and engage in positive behaviors to help coping. Scores are on a four-point scale (1 to 4) with a total available score of 12. Higher scores indicate greater self-efficacy.

  5. Care experiences will be analyzed as a change over time [Baseline (immediately following loss), 4 weeks and 8 weeks post loss]

    11 items of experiences of care at the time of loss and follow-up appointments after loss. Responses on a 4-point scale (1 to 4) to indicate level of agreement with a total available score of 44. Higher scores indicating better experiences.

  6. Usability [Post-Treatment (8 weeks post loss)]

    The System Usability Scale is commonly used 10-item scale that measures subjective perceptions of usability on a 5-point Likert-scale. The participant's scores for each question are converted to a new number, added together and then multiplied by 2.5 to convert the original scores of 0-40 to 0-100. Higher scores indicate the technology is more usable.

  7. Acceptability [Post-Treatment (8 weeks post loss)]

    Developed as part of the current study. Items developed to measure the degree, on a 7-point Likert-type scale, to which parents found the program helpful, acceptable, and suited to their needs. Higher scores will indicate greater acceptability.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusions Criteria

Focus Groups and Usability Testing (Bereaved Parents)

  • Experienced a perinatal loss

  • Have had at least 6 months pass since experiencing the most recent loss

  • Age 15 and older

Efficacy Study (Bereaved Parents)

  • Bereaved parent who has experienced a perinatal loss within the last two weeks * Age 15 and older

  • Have access to technology to view WWM content

Exclusion Criteria

  • Non-English speakers are excluded. The WWM program will first be developed in English and its feasibility established.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Oregon Research Behavioral Intervention Strategies, Inc. Eugene Oregon United States 97403

Sponsors and Collaborators

  • Oregon Research Behavioral Intervention Strategies, Inc.

Investigators

  • Principal Investigator: Camille C Cioffi, PhD, Oregon Research Behavioral Intervention Strategies, Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Oregon Research Behavioral Intervention Strategies, Inc.
ClinicalTrials.gov Identifier:
NCT05318287
Other Study ID Numbers:
  • MH126788
First Posted:
Apr 8, 2022
Last Update Posted:
Apr 8, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 8, 2022