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Completed

NCT Number: NCT03474172

Development and Validation of a Cloak Shape Device for Sham Pediatric Tuina

This study aims to evaluate the effectiveness of a Cloak Shape sham Pediatric Tuina device which can be applied in randomized controlled trials for Pediatric Tuina research.

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Key information

Conditions

Age range

Up to 6 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dongguan Kanghua Hospital

Dongguan, Guangdong, 523080, China

About this study

Chinese pediatric Tuina has been practiced as an option for health promotion, including disease prevention and treatment, more than one thousand years ago (652 AD). Many of the acupoints adopted in Chinese pediatric Tuina are located on children's fingers, hands and arms, which are unique if it is compared with those for adult tuina. The manipulation is found to be easily accepted by children, as the strength of tuina is gentle and soft. No severe adverse reaction in regards of Chinese pediatric Tuina was reported, the mild adverse reaction such as skin abrasion can be completely avoided with correct operating instructions. However, it is still lack of high quality RCTs (Randomized Controlled Trials) to evaluate its efficacy. The main obstacle is the difficulty to conduct a valid sham Tuina comparison group. In order to solve this problem, the investigators designed a device for sham Tuina, with a Cloak Shaped cover which is opaque and big enough to cover the whole body and arms of a child who is under 6 years old. Two narrow holes are required on the cover, so that the therapist's hands can touch the child through these holes. The whole manipulation process will be invisible under the cover.The investigators aim to detect whether it is effective as a sham device for pediatric Tuina researches.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children with disease in Pediatric Outpatient Department of Kanghua Hospital
  • Children aged 0-6 years.
  • Guardian and child can be cooperative over the study period.
  • Guardian signed the informed consent.
  • Children have no attendance in other studies simultaneously.

Exclusion criteria

  • Child with one or more PT experiences on arms, abdomen or back.
  • Child with a previous history of convulsion.
  • Child with any of the following conditions on the area to be manipulated: phlebitis, open wound, fracture and tissue damage.
  • Child combined with any of following conditions: disorders of consciousness, seizures or twitching, shock, varicella, hand-foot-mouth disease, encephalitis B, and etc.

Treatment and study plan

Cloak Shape Device for Sham Tuina

Device

The Cloak Shape Device for Sham Tuina is exactly the same as the real one, which is opaque and big enough to cover the whole body and arms of a child who is under 6 years old. Two narrow holes are required on the cover, so that the therapist's hands can touch the child through these holes and a sham Tuina will be manipulated

Cloak Shape Device for Genuine Tuina

Device

The Cloak Shape Device for Genuine Tuina is opaque and big enough to cover the whole body and arms of a child who is under 6 years old. Two narrow holes are required on the cover, so that the therapist's hands can touch the child through these holes and a genuine Tuina will be manipulated.

Primary outcomes

  1. The Accuracy Judgement Rates of the Type of Tuina That Children Received Based on Parents' Evaluations

    Time frame: The outcome measures started right after the PT therapy was completed and the measurement lasted for 10-15 mins.

    The accuracy judgement rate was calculated from the original data as below and was used as the primary outcome in the study.

  2. The Accuracy Judgement Rates of the Type of Tuina That Children Received Based on Observers' Evaluations

    Time frame: The outcome measures started right after the PT therapy was completed and the measurement lasted for 10-15 mins.

    The accuracy judgement rate was calculated from the original data as below and was used as the primary outcome in the study.

Secondary outcomes

  1. Verbal Rating Scale (VRS) of Parent's Attitude Towards Pediatric Tuina

    Time frame: The outcome measures started right after the PT therapy was completed and the measurement lasted for 10-15 mins.

    We adopt the VRS-4 to indicate diferent confident intensities towards pediatric Tuina from the perspective of parents as follow: not confident, somewhat confident, confident ,very confident.

  2. Verbal Rating Scale (VRS) of Children's (≥3 Years Old) Perception of Pediatric Tuina

    Time frame: The outcome measures started right after the PT therapy was completed and the measurement lasted for 10-15 mins.

    We adopt the VRS-5 to indicate diferent discomfort intensities towards pediatric Tuina from the perspective of children equal or larger than 3 years old during and after the Tuina as follow: no discomfort; some discomfort; discomfort; very uncomfortable ; uncertain.

  3. VRS of Parent's Attitude Towards Pediatric Tuina From the Observers' Perspectives

    Time frame: The outcome measures started right after the PT therapy was completed and the measurement lasted for 10-15 mins.

    We adopt the VRS-4 to indicate diferent trust intensities of the parents towards pediatric Tuina from the perspective of observers' perspectives as follow: Not confident, somewhat confident, confident, very confident.

  4. Compliance of Guardians and Children for Three Continuous PT Therapies

    Time frame: The outcome measures started right after the PT therapy was completed and the measurement lasted for 10-15 mins.

    We adopt the VRS-4 to indicate diferent compliance intensities to follow 3 days continuous Tuina therapies as follow:improbable, somewhat improbable, probable, very probable.

Sponsors and collaborators

Lead sponsor

Guangzhou University of Traditional Chinese Medicine

Other

Collaborators

  • Dongguan Kanghua Hospital

Registry information

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Mar 22, 2018
Registry last updated
Mar 10, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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