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Continuous shortwave diathermy with physiotherapy for chronic low back pain: trial protocol detailsTrial Plans to Test Shortwave Diathermy for Chronic Back Pain

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Key Takeaway
Note that this is a study protocol; no clinical outcomes or safety data are currently available for chronic low back pain.

The proposed randomized sham-controlled trial aims to evaluate the efficacy of continuous shortwave diathermy (CSWD) combined with a standardized physiotherapy program for 208 adults aged 18 to 65 years with chronic low back pain. The study will be conducted in tertiary hospitals and physiotherapy clinics in Dhaka, Bangladesh.

The intervention group will receive CSWD at 27.12 MHz in continuous mode for 20 minutes per session, three times weekly for four weeks, alongside a standardized physiotherapy program. The comparator group will receive sham CSWD combined with the same standardized physiotherapy program.

The primary outcomes are back pain intensity, leg pain intensity (measured on a 0 to 10 numerical rating scale), and activity limitation (Oswestry Disability Index). Secondary outcomes include Brief Pain Inventory, Global Rating of Change, Satisfaction with Treatment, DASS-21, Insomnia Severity Index, Treatment Credibility Questionnaire, and healthcare utilization. Follow-up assessments are planned for 4, 12, and 24 weeks.

Because this is a study protocol, no results regarding efficacy or safety have been reported. Clinical application of these findings remains pending the completion of the trial.

Researchers are preparing a study to evaluate how continuous shortwave diathermy (CSWD) affects people living with chronic low back pain. The study will involve 208 adults between the ages of 18 and 65 who are seeking relief from persistent back discomfort.

The plan involves comparing two groups: one receiving CSWD combined with a standard physiotherapy program, and another receiving a sham (placebo) version of the heat treatment along with the same physiotherapy. The goal is to see if the specific heat treatment provides extra benefits for pain intensity and daily activity.

Because this is currently a study protocol, no results have been collected or reported yet. This means the findings cannot be used to recommend a specific treatment at this time. Once the trial is complete, the data will help doctors in Bangladesh decide if this type of heat therapy is an effective tool for their patients.

What this means for you:
This is a planned study; results are not yet available to determine if the treatment is effective.

Common questions

Is this treatment currently proven to work for back pain?

Because the study is currently in the protocol phase, no results have been reported yet. We cannot say if it works until the trial is completed and the data is analyzed by the researchers.

Who is eligible for this specific study?

The planned study is designed for 208 adults between the ages of 18 and 65 who are experiencing chronic low back pain in a clinical setting.

What exactly is being compared in the trial?

The study compares a program of physiotherapy combined with continuous shortwave diathermy against a program of physiotherapy combined with a sham (placebo) version of the heat treatment.

Study Details

Study typeRct
Sample sizen = 208
EvidenceLevel 2
Follow-up780.0 mo
PublishedJan 2026
View Original Abstract ↓
BACKGROUND: Chronic low back pain (CLBP) is a leading cause of disability worldwide and a major public health concern in low- and middle-income countries such as Bangladesh. Although international guidelines classify shortwave diathermy as a low-value treatment, it remains widely used in physiotherapy practice. Evidence on the effectiveness of continuous shortwave diathermy (CSWD) for CLBP is limited and inconsistent. This study aims to determine whether CSWD, when combined with standard physiotherapy, provides additional benefits compared with sham CSWD plus physiotherapy. METHODS: This multicentre, randomised, single-blind, sham-controlled trial will recruit 208 participants aged 18-65 years with CLBP from tertiary hospitals and physiotherapy clinics in Dhaka, Bangladesh. Participants will be randomly allocated (1:1) to receive CSWD or sham CSWD, each combined with a standardised physiotherapy programme delivered three times weekly for four weeks. The intervention group will receive active CSWD (27.12 MHz, continuous mode, 20 min/session), while the control group will receive sham treatment. Primary outcomes include back pain intensity, leg pain intensity (0-10 numerical rating scale), and activity limitation (Oswestry Disability Index). Secondary outcomes include the Brief Pain Inventory, Global Rating of Change, Satisfaction with Treatment, DASS-21, Insomnia Severity Index, Treatment Credibility Questionnaire, and healthcare utilisation. Outcomes will be assessed at baseline, 4, 12, and 24 weeks. Data will be analysed using an intention-to-treat approach with linear mixed-effects models. DISCUSSION: This trial will provide high-quality, context-specific evidence on the clinical and cost-effectiveness of CSWD for CLBP in a resource-constrained setting. The findings will inform physiotherapy practice in Bangladesh and may guide the appropriate use or de-implementation of this commonly used modality. The rigorous sham-controlled design will also contribute to the broader evidence base on electrotherapy for chronic pain.
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