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Effects of Digital Stories Intervention on Psychosocial Well-being

Arizona State University (ASU) logo

Arizona State University (ASU)

Status

Completed

Conditions

Bone Marrow Transplant
Narrative
Psychosocial Health
Hematopoietic Stem Cell Transplantation
Depression
Anxiety
Information Disclosure
Stress

Treatments

Behavioral: Information Control Intervention
Behavioral: Baseline Surveys
Behavioral: Digital Stories Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03654599
R15CA213035 (U.S. NIH Grant/Contract)
GR11968

Details and patient eligibility

About

Patients and caregivers undergoing hematopoietic stem cell transplantation often continue to experience anxiety, depression, isolation, and other psychosocial distress. A narrative-based digital stories intervention has shown promise in a pilot study with breast cancer patients in helping to alleviate emotional distress. This study is designed to test digital stories to be viewed and discussed by other HCT patients/caregivers as a psychosocial intervention in a randomized controlled trial and to test the effects of digital stories on how 110 patient and caregiver dyads (N=220) undergoing one of the most rigorous and aggressive treatments cope with treatment-related distress through supportive open dyadic communication and emotional expression.

Full description

Patients and caregivers undergoing hematopoietic stem cell transplantation (HCT) are at particular risk for reduced psychological and social well-being due to the rigorous and unique nature of the transplant experience, such as prolonged immunosuppression and multiple post HCT complications resulting in frequent hospitalizations. However, few studies have evaluated interventions to alleviate psychosocial distress for both patients and caregivers, and those have yielded inconclusive results. A narrative-based (storytelling) approach may be an effective intervention tool for HCT patients and caregivers coping with psychosocial distress. The preliminary data show that stories shared by individuals in which a range of emotional expression or resolutions are described, may have beneficial effects on emotional well-being. In a recent pilot study of a 3-day digital storytelling workshop, investigators produced a series of digital videos with narratives from a panel of post-HCT patients. The purpose of this study is to use these digital stories (DS), to be viewed and discussed by HCT patient/caregiver dyads, as a therapeutic intervention and to examine influences on both patients' and caregivers' psychosocial status. This cost-effective, non-invasive, and easy-to-deliver psychosocial support vehicle has never been formally tested as an intervention for HCT patients or patient-caregiver dyads.

To build upon investigators' preliminary studies and to pilot test the efficacy of this series of DS, 110 adult patients undergoing HCT at the Mayo Clinic Arizona and patient respective adult caregivers (N=220 total participants) will be randomized to either (a) an intervention using DS (dyadic exposure to four 5-minute modules) or (b) an information control (IC) video group (dyadic exposure to four videos containing only information about post-HCT care) followed by encouragement to discuss as a dyad. Exposure will occur once per week over 4 weeks via a secure web-based data collection platform (REDcap) with a weekly email notification and reminder phone call. Using investigator's model of Narrative Effects on Socio-Emotional Well-Being, we will also examine expected mediating factors to determine how stories may "work" to reduce psychosocial distress by fostering emotional processing, acceptance, and dyadic disclosure of emotions.

Enrollment

202 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Patient Inclusion Criteria:

  • age 18 or older
  • recently underwent Hematopoietic cell transplantation (HCT) (within a month after hospital discharge)
  • must be able to speak, read, and write in English
  • access to a working phone and e-mail account

Patient Exclusion Criteria:

  • no primary caregiver
  • cognitive impairment that prohibits completion of study assessment
  • visual or hearing impairment
  • other (e.g., provider non-approval or logistical constraints such as patient moving out of town)

Caregiver Inclusion Criteria:

  • age 18 or older
  • family caregivers who are identified as a primary caregiver by a patient
  • have primary responsibility for the care of patients throughout the HCT process
  • Must be able to speak, read, and write in English
  • Access to a working phone and e-mail account

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

202 participants in 4 patient groups

Baseline and Digital Stories (DS) for patients
Experimental group
Description:
In-person baseline surveys using the web-based data collection platform, Research Electronic Data Capture before the random assignment to DS arm. Eight Digital Stories Intervention (4 patient and 4 caregiver stories about hematopoietic stem cell transplantation (HCT) over the course of 4 weeks (2 videos per week) with a weekly email notification and reminder phone call. Each story was made with voice, images, and sound (3-5 minutes each).
Treatment:
Behavioral: Digital Stories Intervention
Behavioral: Baseline Surveys
Baseline and Information Control (IC) for patients
Active Comparator group
Description:
In-person baseline surveys using the web-based data collection platform, Research Electronic Data Capture (REDCap) before the random assignment to IC arm. Eight Information Control Intervention videos containing only information about post-HCT care (as opposed to story/narrative) over the course of 4 weeks (2 videos per week) with a weekly email notification and reminder phone call.
Treatment:
Behavioral: Baseline Surveys
Behavioral: Information Control Intervention
Baseline and Digital Stories (DS) for caregivers
Experimental group
Description:
In-person baseline surveys using the web-based data collection platform, Research Electronic Data Capture before the random assignment to DS arm. Eight Digital Stories Intervention (4 patient and 4 caregiver stories about hematopoietic stem cell transplantation (HCT) over the course of 4 weeks (2 videos per week) with a weekly email notification and reminder phone call. Each story was made with voice, images, and sound (3-5 minutes each).
Treatment:
Behavioral: Digital Stories Intervention
Behavioral: Baseline Surveys
Baseline and Information Control (IC) for caregivers
Active Comparator group
Description:
In-person baseline surveys using the web-based data collection platform, Research Electronic Data Capture (REDCap) before the random assignment to IC arm. Eight Information Control Intervention videos containing only information about post-HCT care (as opposed to story/narrative) over the course of 4 weeks (2 videos per week) with a weekly email notification and reminder phone call.
Treatment:
Behavioral: Baseline Surveys
Behavioral: Information Control Intervention

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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