Comparison of Abdominal Expansion and Abdominal Drawing-In Training With Manual and Verbal Cueing in Chronic Non-Specific Low Back Pain

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Yang Ming Chiao Tung University

About this trial

This study aims to investigate the interactive effects of two core stability training strategies-abdominal drawing-in manoeuvre (ADIM) and Dynamic Neuromusculoskeletal Stabilization abdominal expansion (DNS-AE)-and two instructional approaches (verbal cueing and manual facilitation) on training outcomes in individuals with chronic non-specific low back pain.

A 2×2 factorial randomized controlled trial design will be employed. Ninety-six participants with chronic non-specific low back pain will be randomly allocated, using block randomization, to one of four intervention groups in equal proportions. All groups will receive a 4-week intervention program, with training conducted twice per week.

Outcome measures will be assessed at four time points: before the intervention (baseline), immediately after the first training session, at the completion of the 4-week intervention, and at a 3-month follow-up, to evaluate short-term and mid-term effects as well as the sustainability of training outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 18 years or older.

Clinically diagnosed with chronic non-specific low back pain, with symptoms persisting for more than 12 weeks.

Able to understand the study procedures and comply with the full intervention and assessment protocol.

Disqualifiers

History of surgery involving the lower back or lower extremities.

Presence of neurological symptoms, such as numbness or tingling sensations.

Signs or symptoms of nerve root compression.

History of any surgical procedure within the past 3 months.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Abdominal Drawing-In Manoeuvre Training

    Behavioral

    Abdominal drawing-in manoeuvre (ADIM) training is a core stability exercise strategy emphasizing selective activation and coordination of the deep abdominal musculature to enhance local trunk stability. Participants receive individualized, one-on-one training delivered by licensed physical therapists, conducted twice weekly for 4 weeks. Training is performed across functional positions and task-specific movements, with instruction provided using either verbal cueing or manual facilitation according to group allocation.

  • Dynamic Neuromusculoskeletal Stabilization Abdominal Expansion Training

    Behavioral

    Dynamic Neuromusculoskeletal Stabilization abdominal expansion (DNS-AE) training focuses on coordinated breathing and abdominal expansion to facilitate intra-abdominal pressure regulation and integrated postural control. Participants receive individualized, one-on-one training delivered by licensed physical therapists, conducted twice weekly for 4 weeks. Training is performed across functional positions and task-specific movements, with instruction provided using either verbal cueing or manual facilitation according to group allocation.

Treatment groups

96 Participants
are divided into 4 treatment groups
Group A: ADIM With Verbal CueingExperimental treatment 1 intervention
Group B: ADIM With Manual CueingExperimental treatment 1 intervention
Group C: DNS-AE With Verbal CueingExperimental treatment 1 intervention
Group D: DNS-AE With Manual CueingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain intensity

Pain intensity assessed using the Visual Analogue Scale (VAS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable, with higher scores indicating greater pain intensity.

Time frame
At baseline, after the first week of intervention, and at the end of the 4-week intervention.
2

Movement control performance

Movement control performance assessed using the Nine-Item Movement Control Test Battery, which evaluates movement quality during standardized functional movement tasks. Each item is scored according to predefined error-based criteria, and item scores are summed to produce a total score ranging from 0 to 93, with higher scores indicating poorer movement control performance.

Time frame
At baseline, after the first week of intervention, and at the end of the 4-week intervention.

Secondary outcomes

1

Disability related to low back pain

Disability assessed using the Oswestry Disability Index (ODI), with total scores ranging from 0 %to 100%, where higher scores indicate greater disability.

Time frame
At baseline, at the end of the 4-week intervention, and at 3-month follow-up.
2

Patient-specific functional ability

Functional ability assessed using the Patient-Specific Functional Scale (PSFS), with scores ranging from 0 to 10, where 0 indicates inability to perform the activity and 10 indicates the ability to perform the activity at the pre-injury or normal level, with higher scores indicating better functional ability.

Time frame
At baseline, at the end of the 4-week intervention, and at 3-month follow-up.
3

Perceived movement difficulty assessed using the Perceived Difficulty Index (PDI).

Perceived difficulty during movement performance assessed using the Perceived Difficulty Index (PDI). Participants rate the level of difficulty experienced during the movement tasks on a numeric rating scale ranging from 0 to 10, where 0 indicates no perceived difficulty and 10 indicates extreme difficulty, with higher scores indicating greater perceived difficulty.

Time frame
At baseline, after the first week of intervention, and at the end of the 4-week intervention.
4

Central sensitization symptoms

Symptoms related to central sensitization assessed using the Central Sensitization Inventory (CSI), with total scores ranging from 0 to 100, where higher scores indicate greater symptom severity related to central sensitization.

Time frame
At baseline and at the end of the 4-week intervention.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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