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Acupuncture in Infantile Colic - a Three Armed Randomized Multi Center Trial (ACU-COL) (ACU-COL)

Primary Purpose

Infantile Colic

Status
Completed
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
Acupuncture
Sponsored by
Lund University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infantile Colic focused on measuring infant, colic, crying, acupuncture, stooling, sleep

Eligibility Criteria

2 Weeks - 8 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • otherwise healthy infants
  • crying/fussing more than three hours/day more than three days in the same week
  • has tried cow´s milk protein free diet for at least five days

Exclusion Criteria:

  • born before week 36
  • has tried acupuncture treatment
  • dont gain weight properly
  • taking other medicine than dimethicone or lactobacillus reuteri
  • parents who don´t understand Swedish

Sites / Locations

  • Arlöv vårdcentral, BVC
  • Askims vårdcentral, BVC
  • Tullgårdens BVC
  • Valla Vårdcentral, BVC

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Group A: Standardized acupuncture

Group B: Individualized acupuncture

Group C: No acupuncture

Arm Description

Infants come to the clinic twice a week for three weeks. Parents meet a nurse and hand the infant to her. The nurse brings the infant to a room where another nurse, trained in acupuncture, is alone with the infant for five minutes. Intervention: Infants in the standardized acupuncture group get minimal acupuncture: one needle is inserted about 3 mm in the point LI4 on the infants hands, unilaterally, for 2-10 seconds and then withdrawn.

Infants come to the clinic twice a week for three weeks. Parents meet a nurse and hand the infant to her. The nurse brings the infant to a room where another nurse, trained in acupuncture, is alone with the infant for five minutes. Infants in the individualized acupuncture group get acupuncture in points chosen by the acupuncturists according to symptoms: maximum 5 needles are inserted about 3 mm in points recommended in a guideline produced for the trial. Needles are retained for maximum one minute.

Infants come to the clinic twice a week for three weeks. Parents meet a nurse and hand the infant to her. The nurse brings the infant to a room where another nurse, trained in acupuncture, is alone with the infant for five minutes. The nurse hold the infant´s hand and talks to it but no acupuncture is given.

Outcomes

Primary Outcome Measures

change in crying
Difference over time and between groups in reduction in % of colicky crying, crying and fussing in minutes/day

Secondary Outcome Measures

change in stooling
The frequency of stooling per day

Full Information

First Posted
December 29, 2012
Last Updated
June 25, 2016
Sponsor
Lund University
Collaborators
Ekhagastiftelsen
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1. Study Identification

Unique Protocol Identification Number
NCT01761331
Brief Title
Acupuncture in Infantile Colic - a Three Armed Randomized Multi Center Trial (ACU-COL)
Acronym
ACU-COL
Official Title
Acupuncture in Infantile Colic - a Three Armed Randomized Multi Center Trial Comparing Acupuncture in a Standardized Point, Acupuncture in Individually Chosen Points and no Acupuncture
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
May 2015 (Actual)
Study Completion Date
May 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lund University
Collaborators
Ekhagastiftelsen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this prospective randomized three armed, multi center study is to compare the effect of two types of acupuncture and no acupuncture in 2-8 weeks old infants with infantile colic. Group A will get standardized minimal acupuncture in LI4, group B will get individualized acupuncture in different points according to symptoms and group C will not get acupuncture. Parents (who register the infants crying) and the nurse they meet at the study CHC are blinded.
Detailed Description
Infantile colic is a common problem, affecting 10-20% of newborns. Both the baby and the parents are suffering and there is a risk that the early relationship is disturbed. There is no safe and effective drug and the use of complementary medicine is increasing in spite of weak or no evidence. Acupuncture releases different neurotransmitters and hormones, is calming, gives pain reduction and affects digestion. Therefore it is reasonable that acupuncture can have effect in colic. Acupuncture in infantile colic has shown promising results in the few scientific trials conducted. These trials have evaluated the effect of standardized minimal acupuncture in the acupuncture points Large Intestine 4 (LI4) (two trials) or Stomach 36 (ST36) (one recent trial). In this prospective randomized three armed, multi center study performed at Child Health Centers in three towns, the effect of acupuncture in reducing symptoms in infants, 2-8 weeks old, with colic will be investigated. Two types of acupuncture: standardized minimal acupuncture in LI4 and individualized acupuncture in different points according to symptoms will be compared to an untreated group. Parents (who register the infants crying) and the nurse they meet at the study CHC are blinded. Parents will get information about the trial from nurses and doctors at Child Health Centers (CHC) or from a web-site (www.spädbarnskolik.se). Parents who are interested in letting their infant participate in the trial get further information and sign informed consent. The trial is approved by the ethical board at Lund University. Infant´s crying, fussing, sleep, feeding and stooling will be registered in a diary during a baseline week. Infants who cry/fuss more than three hours/day, more than three days during this week is included and randomized. Beside their ordinary contacts with their Child Health Center (CHC), infants and their parents are invited to visit a study CHC twice a week for two weeks, where they meet a nurse for about 20 minutes. Parents can describe their situation, discuss the infant´s symptoms and get advice. This nurse is blinded to which group the infant is randomized to. She carries the baby to another room and hands over the infant to a nurse, trained in acupuncture. The acupuncture nurse randomizes the infants to one of three groups, following a randomization list produced by the research department at Lund University Hospital. Group A will get standardized minimal acupuncture: one needle is inserted about 3 mm in the point LI4 on the infants hands, unilaterally, for 2-10 seconds and then withdrawn. Group B will get individualized acupuncture in points chosen by the acupuncturists according to symptoms: maximum 5 needles are inserted about 3 mm in points recommended in a guideline produced for the trial after discussions with experienced pediatric acupuncturists. Needles are retained for maximum one minute. Group C will not get acupuncture but will otherwise be treated similarly: they will be with the acupuncture nurse for five minutes while she holds the hand of the baby and talks to it in a calm voice. The acupuncture nurse make notes about bleeding and other possible side effects, and if the baby is crying. After approximately five minutes the acupuncture nurse calls the study nurse who carries the baby back to the parents. At every visit the study nurse asks parents if they have noticed any side effects, and asks if parents believe their baby gets acupuncture or not. During the two intervention weeks and one week after the last visit to the study CHC parents register the infants behavior daily in a diary. Statistical analyses will be made from the diaries.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infantile Colic
Keywords
infant, colic, crying, acupuncture, stooling, sleep

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
147 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A: Standardized acupuncture
Arm Type
Active Comparator
Arm Description
Infants come to the clinic twice a week for three weeks. Parents meet a nurse and hand the infant to her. The nurse brings the infant to a room where another nurse, trained in acupuncture, is alone with the infant for five minutes. Intervention: Infants in the standardized acupuncture group get minimal acupuncture: one needle is inserted about 3 mm in the point LI4 on the infants hands, unilaterally, for 2-10 seconds and then withdrawn.
Arm Title
Group B: Individualized acupuncture
Arm Type
Active Comparator
Arm Description
Infants come to the clinic twice a week for three weeks. Parents meet a nurse and hand the infant to her. The nurse brings the infant to a room where another nurse, trained in acupuncture, is alone with the infant for five minutes. Infants in the individualized acupuncture group get acupuncture in points chosen by the acupuncturists according to symptoms: maximum 5 needles are inserted about 3 mm in points recommended in a guideline produced for the trial. Needles are retained for maximum one minute.
Arm Title
Group C: No acupuncture
Arm Type
No Intervention
Arm Description
Infants come to the clinic twice a week for three weeks. Parents meet a nurse and hand the infant to her. The nurse brings the infant to a room where another nurse, trained in acupuncture, is alone with the infant for five minutes. The nurse hold the infant´s hand and talks to it but no acupuncture is given.
Intervention Type
Other
Intervention Name(s)
Acupuncture
Intervention Description
Minimal standardized acupuncture: one needle is inserted about 3 mm in the point LI4 on the infants hands, unilaterally, for 2-10 seconds and then withdrawn. Individualized acupuncture: maximum 5 needles are inserted, about 3 mm deep, in points chosen by the acupuncturists according to symptoms, in points recommended in a guideline produced for the trial. Needles are retained for maximum one minute.
Primary Outcome Measure Information:
Title
change in crying
Description
Difference over time and between groups in reduction in % of colicky crying, crying and fussing in minutes/day
Time Frame
mean values for crying during the baseline week, during each of the two intervention weeks and during the week after the last treatment
Secondary Outcome Measure Information:
Title
change in stooling
Description
The frequency of stooling per day
Time Frame
mean values for stooling during the baseline week, during each of the two intervention weeks and during the week after the last treatment
Other Pre-specified Outcome Measures:
Title
Change in hours of sleep
Description
Hours of sleep per day
Time Frame
mean values for sleep and length of undisturbed sleep during the baseline week, during each of the two intervention weeks and during the week after the last treatment
Title
side effects
Description
At each visit parents will be asked by the study nurse whether they have noticed any side effects that they believe can be associated with acupuncture. One week after the last visit they will, by telephone, be asked the same question by the study coordinator.
Time Frame
each of the four visits to the study CHC and one week after the last visit
Title
Blinding
Description
At each visit parents will be asked by the study nurse whether they believe that their infant is allocated to acupuncture or not. One week after the last visit they will, by telephone, be asked the same question by the study coordinator.
Time Frame
each of the four visits to the study CHC and one week after the last visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Weeks
Maximum Age & Unit of Time
8 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: otherwise healthy infants crying/fussing more than three hours/day more than three days in the same week has tried cow´s milk protein free diet for at least five days Exclusion Criteria: born before week 36 has tried acupuncture treatment dont gain weight properly taking other medicine than dimethicone or lactobacillus reuteri parents who don´t understand Swedish
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kajsa Landgren, PhD
Organizational Affiliation
Lund University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Arlöv vårdcentral, BVC
City
Arlöv
State/Province
Skåne
ZIP/Postal Code
232 38
Country
Sweden
Facility Name
Askims vårdcentral, BVC
City
Askim
State/Province
Västra Götaland
ZIP/Postal Code
436 32
Country
Sweden
Facility Name
Tullgårdens BVC
City
Karlskrona
ZIP/Postal Code
371 85
Country
Sweden
Facility Name
Valla Vårdcentral, BVC
City
Linköping
State/Province
Östergötland
ZIP/Postal Code
582 16
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32375501
Citation
Landgren K, Hallstrom I, Tiberg I. The effect of two types of minimal acupuncture on stooling, sleeping and feeding in infants with colic: secondary analysis of a multicentre RCT in Sweden (ACU-COL). Acupunct Med. 2021 Apr;39(2):106-115. doi: 10.1177/0964528420920308. Epub 2020 May 6.
Results Reference
derived
PubMed Identifier
28093383
Citation
Landgren K, Hallstrom I. Effect of minimal acupuncture for infantile colic: a multicentre, three-armed, single-blind, randomised controlled trial (ACU-COL). Acupunct Med. 2017 Jun;35(3):171-179. doi: 10.1136/acupmed-2016-011208. Epub 2017 Jan 16.
Results Reference
derived
PubMed Identifier
26370560
Citation
Landgren K, Tiberg I, Hallstrom I. Standardized minimal acupuncture, individualized acupuncture, and no acupuncture for infantile colic: study protocol for a multicenter randomized controlled trial - ACU-COL. BMC Complement Altern Med. 2015 Sep 14;15:325. doi: 10.1186/s12906-015-0850-x.
Results Reference
derived

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Acupuncture in Infantile Colic - a Three Armed Randomized Multi Center Trial (ACU-COL)

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