Balance Impairment, Lower Limb Amputation, Mobility Limitations, Prosthesis Users
Conditions
Keywords
Dual-task training, Balance training, Lower-limb prosthesis, Traumatic amputation, Amputee rehabilitation, Berg Balance Scale, Amputee Mobility Predictor, DASS-21, Gaza Strip, Mental health
Brief summary
This randomized controlled trial will evaluate the effectiveness of dual-task balance training on balance, mobility, and mental health among traumatic lower-limb prosthesis users in the Gaza Strip. Participants will be randomly assigned to either an experimental group receiving dual-task balance training in addition to standard rehabilitation or a control group receiving standard rehabilitation only. The intervention will be delivered over 6 weeks, with three sessions per week. Balance and mobility will be assessed using the Berg Balance Scale and the Amputee Mobility Predictor with Prosthesis, while mental health will be assessed using the Depression, Anxiety, and Stress Scale-21.
Detailed description
Lower-limb amputation can lead to significant impairments in balance, mobility, functional independence, and psychological well-being. Prosthesis users often experience challenges during walking and daily activities, particularly when they are required to perform a motor task and a cognitive task at the same time. Dual-task balance training is a rehabilitation approach that combines balance exercises with concurrent cognitive or motor tasks to improve postural control, mobility, attention, and functional performance. This study is a parallel-group randomized controlled trial designed to investigate the effectiveness of dual-task balance training among traumatic lower-limb prosthesis users in the Gaza Strip. Eligible participants will be traumatic transtibial or transfemoral lower-limb prosthesis users who meet the study inclusion criteria and provide informed consent. Participants will be randomly allocated into two groups. The experimental group will receive dual-task balance training in addition to standard rehabilitation. The control group will receive standard rehabilitation only. The dual-task balance training program will be conducted for 6 weeks, with three sessions per week. Training will include progressive balance activities combined with cognitive or motor secondary tasks, according to the participant's ability and safety level. The primary outcomes of the study are balance and mobility, measured using the Berg Balance Scale and the Amputee Mobility Predictor with Prosthesis. The secondary outcome is mental health, measured using the Depression, Anxiety, and Stress Scale-21. Outcome measurements will be collected before and after the intervention period by an assessor who is not involved in delivering the intervention. The study aims to provide evidence on whether adding dual-task balance training to standard rehabilitation can improve balance, mobility, and mental health outcomes among traumatic lower-limb prosthesis users in a resource-limited rehabilitation setting.
Interventions
BEHAVIORALDual-Task Balance Training
A 6-week rehabilitation program consisting of progressive balance training combined with concurrent cognitive or motor tasks. Sessions will be conducted three times per week and will be adapted according to participant ability and safety level.
BEHAVIORALStandard Rehabilitation
Usual rehabilitation care provided for lower-limb prosthesis users, including therapeutic exercises, gait training, balance activities, and functional mobility training according to the participant's clinical needs.
Sponsors
Al-Azhar University - Gaza
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
The outcomes assessor will be blinded to group allocation. Participants and care providers cannot be blinded due to the nature of the rehabilitation intervention.
Intervention model description
Participants will be randomly assigned into two parallel groups. The experimental group will receive dual-task balance training in addition to standard rehabilitation, while the control group will receive standard rehabilitation only. Outcomes will be measured before and after the 6-week intervention period.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adults aged 18 years or older. * Traumatic unilateral lower-limb amputation. * Transtibial or transfemoral amputation level. * Current lower-limb prosthesis user. * Able to stand and walk with the prosthesis, with or without an assistive device. * Medically stable and able to participate in a rehabilitation training program. * Able to understand and follow study instructions. * Provides written informed consent.
Exclusion criteria
* Lower-limb amputation due to dysvascular, congenital, or non-traumatic causes. * Bilateral lower-limb amputation. * Severe cognitive impairment that prevents understanding or following study instructions. * Severe visual, vestibular, neurological, or musculoskeletal condition that significantly affects balance or walking independent of the amputation. * Unhealed residual limb wounds, severe pain, or skin problems that prevent safe prosthesis use. * Uncontrolled medical condition that makes participation unsafe. * Participation in another structured balance training program during the study period.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Balance as Assessed by the Berg Balance Scale | Baseline (Day 0) and Week 6 | Balance will be assessed using the Berg Balance Scale (BBS), which consists of 14 functional balance tasks. The total score ranges from 0 to 56, with higher scores indicating better balance performance. Change in balance will be calculated as the Week 6 score minus the baseline score. |
| Change in Mobility as Assessed by the Amputee Mobility Predictor With Prosthesis | Baseline (Day 0) and Week 6 | Mobility will be assessed using the Amputee Mobility Predictor with Prosthesis (AMPPro), which evaluates functional mobility in lower-limb prosthesis users through 21 mobility tasks. The total score ranges from 0 to 47, with higher scores indicating better functional mobility. Change in mobility will be calculated as the Week 6 score minus the baseline score. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Depression, Anxiety, and Stress Symptoms as Assessed by the Depression Anxiety Stress Scales-21 | Baseline (Day 0) and Week 6 | Mental health symptoms will be assessed using the Depression Anxiety Stress Scales-21 (DASS-21), a 21-item self-report instrument comprising three subscales: depression, anxiety, and stress, with 7 items in each subscale. Each item is scored from 0 to 3. The item scores for each subscale are summed and multiplied by 2, resulting in a score range of 0 to 42 for each subscale. Higher scores indicate greater severity of depression, anxiety, or stress symptoms. Change in each subscale score will be calculated as the Week 6 score minus the baseline score. |
Countries
Palestinian Territories
Contacts
CONTACTRawan Nabil Alessi, MSc Student / BSc PT
Outcome results
None listed