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A Guided Online ACT Intervention Combined With Psychoeducation for People With Spinal Cord Injury

A Guided Online Acceptance and Commitment Therapy (ACT) Intervention Combined With Psychoeducation for People With Spinal Cord Injury: A Preliminary Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04670406
Enrollment
10
Registered
2020-12-17
Start date
2021-05-07
Completion date
2021-08-23
Last updated
2021-09-08

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

Conditions

Psychological Distress, Spinal Cord Injuries

Keywords

Acceptance and Commitment Therapy, Quality of life, Spinal cord injury, Psychological distress, Depression, Anxiety, Stress, Mindfulness, Self-compassion

Brief summary

The purpose of this preliminary study is to examine the effects of a guided online acceptance and commitment therapy (ACT) intervention combined with psychoeducation on people with spinal cord injury (SCI) who experience psychological distress.

Detailed description

This project will employ a one-group pretest-posttest design to investigate the effects of a guided online acceptance and commitment therapy (ACT) intervention combined with psychoeducation on quality of life and mental health of people with spinal cord injury (SCI) who experience psychological distress. After the pretest evaluation, eligible participants will receive 8 weekly sessions, including 6 ACT sessions and 2 psychoeducation sessions, delivered by trained coaches through Zoom videoconferencing. Each session lasts for one hour. Primary outcome measures will be psychological distress measured by the Depression, Anxiety and Stress Scale (DASS)- 21 and Spinal Cord Injury - Quality of Life (SCI-QOL). A one-time interview at the completion of the 8 sessions will be conducted to explore participants' experiences in the sessions.

Interventions

BEHAVIORALacceptance and commitment therapy (ACT) combined with psychoeducation

Participants receive 8 weekly sessions, including 6 ACT sessions and 2 psychoeducation sessions, delivered by trained coaches through Zoom videoconferencing.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* community-dwelling adults (age 18 or over) living in the community who had a spinal cord injury * suffering at least mild symptoms of psychological distress measured by the DASS-21 * having a computer/smartphone with internet access capable of doing web browsing and video-conferencing * being able to provide informed consent by understanding the nature of study participation.

Exclusion criteria

* having cognitive, physical, or sensory deficits, or language barriers (non- English communicator) that impede study participation * receiving a psychological therapy currently * having psychiatric hospitalizations or diagnoses of mental illness in the previous 2 years * taking antipsychotic or anticonvulsant medication at the time of recruitment * having the possibility of study dropouts due to other medical conditions

Design outcomes

Primary

MeasureTime frameDescription
Depression, Anxiety and Stress Scale (DASS) - 21Change from baseline to 8 weeksThe Depression, Anxiety and Stress Scale (DASS)- 21 is a 21-item self report instrument designed to measure the three related negative emotional states of depression, anxiety and stress. Higher scores represent greater symptomatology.
World Health Organization Quality of Life Instruments (WHOQOL-BREF) - psychological health componentChange from baseline to 8 weeksWHOQOL-BREF - psychological health component has 6 items measuring: bodily image and appearance; negative feelings; positive feelings; self-esteem; spirituality / personal beliefs; and thinking, learning, memory and concentration. Higher scores denote higher quality of life in terms of psychological health.

Secondary

MeasureTime frameDescription
Action and Acceptance Questionnaire (AAQ)-IIChange from baseline to 8 weeksThe Action and Acceptance Questionnaire (AAQ)-II is a 7-item self-report questionnaire measuring psychological flexibility. Higher scores indicate poor psychological flexibility.
Cognitive Fusion Questionnaire (CFQ)-7Change from baseline to 8 weeksThe Cognitive Fusion Questionnaire (CFQ)-7 is a 7-item self-report questionnaire measuring cognitive fusion. Higher scores indicate greater levels of cognitive fusion.
Self-Compassion Scale- Short Form (SCS-SF)Change from baseline to 8 weeksSelf-Compassion Scale- Short Form (SCS-SF) has 12 items assessing the relation of self-compassion to positive psychological health. Higher scores indicate higher levels of self-compassion.
Spinal Cord Injury - Quality of Life (SCI-QOL) Resilience Short formChange from baseline to 8 weeksSCI-QOL Resilience Short form has 8 items assessing resilience. Higher scores indicate more resilience.
Mindful Attention Awareness Scale (MAAS)Change from baseline to 8 weeksThe MAAS is a 15-item scale assessing dispositional mindfulness (i.e., open or receptive awareness of and attention to what is taking place in the present). Higher scores reflect higher levels of dispositional mindfulness.
Spinal Cord Injury - Quality of Life (SCI-QOL) Grief and Loss Short formChange from baseline to 8 weeksSCI-QOL Grief and Loss Short form has 9 items assessing grief and loss due to spinal cord injuries. Higher scores indicate more grief/loss.
Engagement in Meaningful Activities Survey (EMAS)Change from baseline to 8 weeksThe Engagement in Meaningful Activities Survey (EMAS) is a 12-item self-assessment instrument that measures a person's subjective experience of the meaningfulness of everyday activities. Higher scores indicate greater levels of engagement in meaningful activities.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026