Effects of a Physical-Psychological Integrative (PPI) Intervention on Physical Inactivity, Depression and Chronic Pain for Community-Dwelling Spinal Cord Injury Survivors: a Pilot Randomized Controlled Trial
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 72
- Locations
- 1
- Primary Endpoint
- Depression at three months follow-up
Study Overview
Brief Summary
Spinal cord injury (SCI) is a neurological disorder that leads to "partial or complete loss of people's motor and/ or sensory function below the level of the injury".
The PPI intervention group participants will indicate significantly greater improvements when compared with those in control group in the minutes of performing the moderate-to-rigorous physical activity, depression, chronic pain and mindfulness skills and quality of life at post-intervention, and three months follow-up. The use of psychological motivational interviewing and online face-to-face meetings will be good modalities for the people with SCI to overcome the barriers of not having face-to-face interactions and transportation problems. And the intervention would be feasible and improve SCI people's physical inactivity, depression and chronic pain as to step up the control of the modifiable risk factors for non-communicable diseases.
Detailed Description
This study is a two-arm, single-blind pilot randomized controlled trial, and it will be adopted to evaluate or compare the effects between the Physical-Psychological Integrative (PPI) intervention group and the brief online didactic education control group.
Seventy-two participants will be recruited from the Hong Kong Direction Association for the Handicapped. 36 people with SCI will be assigned to intervention or control group. Participants in PPI Intervention group will receive a Fitbug wristband activity trackers and exercise bands as an incentive and encouragement for doing more physical exercises. The intervention includes eight weekly online group sessions. Qualitative interviews with the PPI intervention group participants will be conducted to understand their acceptance and perceived strengths and limitations of the intervention programme. While the one in the control group will receive a short video call for general physical and psychological suggestions. This can help to control the contact effects of the PPI intervention. Primary outcomes will be leisure-time physical activity, depression and chronic pain. Secondary outcome will be exercise efficacy.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Care Provider, Outcomes Assessor)
Masking Description
The participants could not be blinded due to the nature of the intervention. Patients will be reminded to keep the intervention content confidential and not discuss this with participants in the control group to avoid contamination. Also, the research assistant (RA1) who responsible for assessing all the outcomes will be blinded to the group allocation.
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •18 years older;
- •Currently living in the community and having SCI for more than 6 months;
- •Complete injury at the C6 or below or incomplete injury at any level ;
- •Having a computer/ smartphone with audio-speaking function and Zoom software, and internet access in a secure place;
- •Using a wheelchair for at least 2 hours a day and having the approval from the physicians to perform exercises;
- •Having no problems in hearing, verbal communication, and vision;
- •Able to communicate in Cantonese and to provide informed consent.
Exclusion Criteria
- •Presented with any significant cognitive impairment or brain injury;
- •Engaged in ongoing psychotherapy or any other physiotherapy/ exercise/ relaxation interventions;
- •Physically active for more than 150 minutes per week;
- •Experiencing significant psychotic symptoms, substance misuse or medically not able for the exercise and psychological programme as diagnosed by their physicians.
Arms & Interventions
The Physical-Psychological Integrative (PPI) intervention group
The PPI intervention will include eight weekly online group sessions (with each session lasts for 60-90 minutes). At the beginning of each online group meeting, the intervention provider will use motivational interviewing techniques to promote participants' adherence to the physical activity program, followed by on-line group psychological intervention
Intervention: Physical-Psychological Integrative Intervention (Behavioral)
The brief online didactic education control group
Participants in the control group will receive a short video call (approximately 20 minutes each week for eight weeks) from the trained research assistant, i.e., RA 2 to provide general physical and psychological suggestions (e.g., encouragement of performing physical activities, and communication skills with family members/friends, and engagement in the community life). This is to control the contact effects of the PPI intervention.
Intervention: Brief online didactic education (Device)
Outcomes
Primary Outcomes
Depression at three months follow-up
Time Frame: Depression will be assessed after three months follow-up.
The 9-item Patient Health Questionnaire (PHQ-9) will be used to measure the participants' depression level.
Leisure-time Physical Activity
Time Frame: Leisure-time Physical Activity will be assessed throughout the study period, an average of two months.
Participants' leisure-time moderated-to-rigorous physical activity (MVPA) will be assessed by using the Fitbug Orb (Chicago, IL) which is a wearable, display, triaxial accelerometer that pairs with Bluetooth with compatible smartphones.
Depression at post-test
Time Frame: Depression will be assessed at post-intervention, an average of two months.
The 9-item Patient Health Questionnaire (PHQ-9) will be used to measure the participants' depression level.
Chronic pain at post test
Time Frame: Chronic pain will be assessed at post-intervention, an average of two months.
An 11-point numerical pain rating scale (NPRS) will be used to measure pain intensity and pain unpleasantness (in the past week), where zero means no pain and 10 means the worst imaginable pain.
Chronic pain at three months follow-up
Time Frame: Chronic pain will be assessed after three months follow-up.
An 11-point numerical pain rating scale (NPRS) will be used to measure pain intensity and pain unpleasantness (in the past week), where zero means no pain and 10 means the worst imaginable pain.
Secondary Outcomes
- Exercise Efficacy at post test(Exercise efficacy will be assessed at post-intervention, an average of two months.)
- QoL: Quality of Life at three months follow up(Quality of Life will be assessed after three months follow-up.)
- Mindfulness at post test(Mindfulness will be assessed at post-intervention, an average of two months.)
- QoL: Quality of Life at post test(Quality of Life will be assessed at post-intervention, an average of two months.)
- Exercise Efficacy at three months follow-up(Exercise Efficacy will be assessed after three months follow-up.)
- Mindfulness at three months follow-up(Mindfulness will be assessed after three months follow-up.)