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Testing SupportGroove: a Novel Mhealth Intervention for Couples Coping with Spinal Cord Injury

Testing SupportGroove: a Novel Mhealth Intervention for Couples Coping with Spinal Cord Injury

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05527691
Enrollment
168
Registered
2022-09-02
Start date
2022-10-03
Completion date
2024-12-30
Last updated
2025-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relationship, Marital, Spinal Cord Injuries

Keywords

spinal cord injuries, couple, relationship, resilience

Brief summary

The purpose of this study is to test the preliminary effects of an 8-week mobile application-based program (SupportGroove) developed for persons with spinal cord injury and their romantic partners.

Detailed description

Eligible couples who provide informed consent will be enrolled in the study and will be randomized to either immediately start the 8-week SupportGroove program or be waitlisted for 8-weeks before starting the program. While actively participating in the program, couples will use the app to engage in daily quests (positive psychology-based activities to be completed on their own or as a couple). Both partners in the participating couple complete self-report assessments at baseline (0 weeks), 8 weeks, 16 weeks, and 28 weeks.

Interventions

BEHAVIORALSupportGroove

An app-delivered program consisting of positive psychology-based activities, such as expressing gratitude, finding meaning, savoring, and fostering connections. Participants complete daily quests suggested through the app, some of which are completed on their own, and some with their partner.

Sponsors

McGuire Research Institute
CollaboratorOTHER
University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* cohabitating romantic couples where one partner has sustained a spinal cord injury at least 3 months prior to enrolling in the study * be able to read and understand printed English instructions * have a smartphone, tablet, or personal computer with internet access

Exclusion criteria

* the partner has a spinal cord injury or other major neurological condition * either partner is unable to read and understand printed English instructions * either partner does not consent to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Spinal Cord Injury Quality of Life (SCI-QOL) Resilience-Short FormBaseline (0 weeks)10-items assessing state resilience; rated from 1-5 (never-always); score range from 19-50, higher score = more resilient /better outcome
Patient Health Questionnaire-90 weeks9-item depression measure; rated from 0-3 (not at all-nearly every day); score range from 0-27, higher scores = more depressed /worse outcome
Spinal Cord Injury Quality of Life (SCI-QOL) Positive Affect and Wellbeing0 weeks10-items assessing aspects of well-being; rated from 1-5 (never-always); score range from 10-50, higher score = greater well-being /better outcome
Revised Dyadic Adjustment Scale0 weeks14-items assessing couple satisfaction and how each partner within the couple perceives their relationship; rated on a scale from 0-5; score range from 0-70, higher scores = better adjustment/greater relationship satisfaction /better outcome

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026