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Laser Acupuncture for Postpartum Weight Retention

Straipsnius versti gali tik registruoti vartotojai
Prisijungti Registracija
Nuoroda įrašoma į mainų sritį
StatusasBaigta
Rėmėjai
Chang Gung Memorial Hospital

Raktažodžiai

Santrauka

Objective: To determine the therapeutic effect of acupuncture on postpartum weight retention.
Methods: 66 subjects after delivery with postpartum weight retention will be randomly divided into laser acupuncture and control group. A single-blind clinical trial will be conducted and the subjects will be treated with verum or sham laser acupuncture 5 sessions per week. After about 3 weeks of treatment, the differences of the subjects' body weight, body mass index, and waist circumference will be analyzed with ANOVA between laser acupuncture and control group.

apibūdinimas

Objective: Gestational weight gain and weight retention at 1 year after delivery are associated with long-term obesity. The investigators aimed to investigate the effect of laser acupuncture therapy (LAT) on postpartum weight control.

Methods: The investigators randomly assigned 66 subjects with postpartum weight retention to a laser acupuncture group and control group. The subjects were treated at acupoints including the Stomach and Hunger points of the ear, ST25 (Tianshu), ST28 (Shuidao), ST40 (Fenglong), SP15 (Daheng), CV9 (Shuifen), and SP6 (Sanyinjiao) by using verum or sham laser acupuncture over 5 sessions per week. After 12 treatment sessions, the differences in the body mass index (BMI), body fat percentage (BFP), and waist-to-buttocks ratio (WBR) of the patients were analyzed, and compared between the laser acupuncture and control groups via analysis of variance, chi-square tests, and stepwise regression tests.

Datos

Paskutinį kartą patikrinta: 10/31/2016
Pirmasis pateikimas: 07/13/2016
Numatytas registravimas pateiktas: 07/18/2016
Pirmas paskelbtas: 07/20/2016
Paskutinis atnaujinimas pateiktas: 11/19/2016
Paskutinis atnaujinimas paskelbtas: 01/15/2017
Pirmųjų rezultatų pateikimo data: 07/22/2016
Pirmojo QC rezultatų pateikimo data: 11/19/2016
Pirmųjų paskelbtų rezultatų data: 01/15/2017
Faktinė studijų pradžios data: 12/31/2013
Numatoma pirminio užbaigimo data: 11/30/2015
Numatoma studijų užbaigimo data: 11/30/2015

Būklė ar liga

Postpartum Weight Retention

Intervencija / gydymas

Procedure: verum laser acupuncture

Procedure: sham laser acupuncture

Fazė

Fazė 3

Rankų grupės

RankaIntervencija / gydymas
Experimental: verum laser acupuncture
verum laser acupuncture
Procedure: verum laser acupuncture
Subjects were treated at acupoints including the Stomach and Hunger points of the ear, ST25, ST28, ST40, SP15, CV9, and SP6 by using laser acupuncture (GaAlAs laser, maximal power, 150 milliwatt; wavelength, 810 nm; area of probe, 0.03 cm2; power density, 5 W/cm2; pulsed wave; 5.625 J/ cm2) over 5 sessions per week, 12 treatment sessions in total.
Sham Comparator: sham laser acupuncture
sham laser acupuncture (no laser output)
Procedure: sham laser acupuncture
Subjects underwent sham laser acupuncture treatment without any laser output. The acupuncture points, application duration, and total number of treatments were similar to those in verum laser acupuncture group.

Tinkamumo kriterijai

Amžius, tinkami studijuoti 20 Years Į 20 Years
Tinkamos studijoms lytysFemale
Priima sveikus savanoriusTaip
Kriterijai

Inclusion Criteria:

- postpartum duration of <1 month;

- body mass index (BMI) > 25;

- age > 20 years;

- did not use any other medications for weight loss during the study period; and

- provided informed consent.

Exclusion Criteria:

- presence of a pacemaker;

- history of seizure or epilepsy;

- taking immunosuppressant medication;

- cancer;

- infectious disease of the skin;

- taking medications for weight loss, including Chinese herbal preparations, during the study period;

- receiving other treatment, including supplements, herbs, and medications for weight gain prior to entering the study;

- comorbidities (hypothyroidism, renal disease, etc.) that the physician believes would affect the findings;

- unable to undergo LAT due to other medical conditions; and

- lack of informed consent.

Rezultatas

Pirminės rezultatų priemonės

1. Body Mass Index (BMI) [up to 3 weeks, 3 months after study completion]

The BMI was assessed by an evaluator who was blinded to the intervention details from the beginning through study completion, up to 3 weeks, and 3 months after study completion.

Antrinės rezultatų priemonės

1. Waist-to-buttock Ratio (WBR) [up to 3 weeks]

The WBR was assessed by an evaluator who was blinded to the intervention details from the beginning through study completion, up to 3 weeks.

2. Body Fat Percentage (BFP) [up to 3 weeks]

The BFP was assessed by an evaluator who was blinded to the intervention details from the beginning through study completion, up to 3 weeks.

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