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Trial registered on ANZCTR

Registration number

ACTRN12614000120673

Ethics application status

Approved

Date submitted

1/01/2014

Date registered

31/01/2014

Date last updated

31/01/2014

Type of registration

Retrospectively registered

Titles & IDs

Public title

Influence of child birthing audiovisuals on anxiety and obstetric outcomes of first time mothers in Ibadan: a randomized controlled trial

Scientific title

Influence of child birthing audiovisuals on anxiety and obstetric outcomes of primigravid women during antenatal clinic in Ibadan: a randomized controlled trial

Secondary ID [1]

NONE

Universal Trial Number (UTN)

Trial acronym

Linked study record

Health condition

Health condition(s) or problem(s) studied:

anxiety level

obstetric outcome

Condition category

Condition code

Reproductive Health and Childbirth

Childbirth and postnatal care

Mental Health

Anxiety

Intervention/exposure

Study type

Interventional

Description of intervention(s) / exposure

Apart from the routine antenatal care service, the intervention group watched a five minutes documentary film on the events that occur during the second stage of labour. This was shown to those in the experimental group after recruitment and assessment of baseline anxiety levels. Questions and clarifications were made during the course of the session to dispel misconceptions and improve knowledge among respondents in the experimental group.

Intervention code [1]

Other interventions

Comparator / control treatment

Only had routine antenatal care service

Control group

Active

Outcomes

Primary outcome [1]

The primary outcome is to measure the change in level of anxiety in the treatment/intervention arm compared to the controls. The State Trait Anxiety Inventory for Adults (STAI) was used to measure the anxiety level.The STAI was administered to assess the state of anxiety and trait anxiety and consists of 20 questions on current feeling of anxiety (state) and usual feeling of anxiety (trait). Feelings of anxiety were rated on a likert scale of 1 (not at all) to 4 (very much so) for each question. Scores were summed, and ranged between 20-80.

Timepoint [1]

assessed at baseline (34 weeks gestation), at 37 weeks gestation and immediately after childbirth

Secondary outcome [1]

The secondary outcome is to measure the change in obstetric outcomes - duration of active phase of labour in hours, mode of delivery (vaginal versus caesarean) and apgar score - for those in the treatment arm compared to those in the control arm

Timepoint [1]

This is monitored on the day of delivery before discharge from the hospital

Eligibility

Key inclusion criteria

1. Primigravid/ nulliparous pregnant women
2. Anticipated vaginal delivery
3. Absence of medical disorders (hypertension, Diabetes Mellitus)
4. Singleton foetus in the current pregnancy
5. 28 -30 weeks gestation

Minimum age

No limit

Maximum age

No limit

Sex

Females

Can healthy volunteers participate?

Yes

Key exclusion criteria

1. Those that decline to participate in the study
2. Presence of multiple pregnancies
3. Fetal malpresentations
4. Other obstetric indications that could contraindicate vaginal delivery

Study design

Purpose of the study

Educational / counselling / training

Allocation to intervention

Randomised controlled trial

Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)

On each clinic day, consenting women that met the inclusion criteria were given serial numbers with allotted treatment group based on their arrival time. Only the RAs had access to the list of numbers used to prevent clinicians’ influence on the randomisation. Each subject opened the opaque envelope in the presence of the RAs, and the assigned treatment group was recorded in the RAs records while an identification number was given and recorded on the medical file. The research protocol was closely monitored by the RAs to avoid bias and also, to ensure that all subjects are assigned to treatment groups. Those administering the proforma and assessing the outcomes were blinded to the groups to which participants belonged.

Methods used to generate the sequence in which subjects will be randomised (sequence generation)

Eligible participants that accepted to be part of the study were recruited into the trial and randomized into two groups. The randomisation sequence was generated using Random Allocation Software, Version 1.0, 2004. Random permuted blocks of size four were used to ensure a balanced design. The blocks are the possible permutations of a sequence of four allocations – two women each belonging to the experimental and control groups. Based on the sequence of treatments generated using this method, treatment groups (A and B) were written on pieces of cardboard paper and put into sealed opaque envelopes. Each of the opaque envelopes had a serial number on it. Two trained research assistants (RAs) non-medical staff supervised the randomisation procedure at every antenatal clinic (ANC).

Masking / blinding

Blinded (masking used)

Who is / are masked / blinded?

The people assessing the outcomes

Intervention assignment

Parallel

Other design features

Phase

Not Applicable

Type of endpoint/s

Efficacy

Statistical methods / analysis

The sample size was calculated with an intention to detect a minimum difference of five in anxiety levels between the groups at 80% power and alpha error of 0.05. This resulted in a sample size of 80. We estimated that about 30% of the women may be lost to follow up, there for sample size was adjusted for and we arrived at 114 (57 in each group). This was rounded up to 120 (60 in each group).

Data collection was done using three instruments (Questionnaire, State Trait Anxiety Inventory and visual analogue scale for anxiety-VAS-A). The questionnaire was an interviewer-administered semi-structured questionnaire consisting of two sections. Section one obtained information on baseline socio demographic characteristics of trial participants, while section two obtained information on the antenatal history.
The State Trait Anxiety Inventory for Adults (STAI) and Visual analogue Scale was used to measure anxiety. The visual analogue for anxiety assessed anxiety level using a standardized pictorial estimate. The State–Trait Anxiety Inventory for Adults (STAI), measures current anxiety and reflects current subjective feelings with respect to tension, apprehension, nervousness, and worry. The STAI was administered to assess the state of anxiety and trait anxiety and consists of 20 questions on present current feeling of anxiety (state) and usual feeling of anxiety (trait). Feelings of anxiety were rated on a scale of 1 (not at all) to 4 (very much so) for each question. Scores were summed, and ranged between 20-80. For all participants enrolled and randomized for the study, baseline information was obtained and anxiety assessment performed using the two scales. Thereafter, serial anxiety assessment was performed for both treatment arms (intervention and control) at 34 weeks, 37 weeks. After childbirth, obstetric/neonatal outcomes and anxiety assessment was done for all participants. This assessment was done by an assessor who was blinded to the groups to which the study participants belonged (intervention and control).

The data was coded, entered, cleaned, and analyzed using Statistical Product and Services Solutions (SPSS) for windows version 18.0.1. Demographic data and clinical characteristics were summarized as the mean +/- standard deviation for continuous variables and as frequency counts (percentages) for categorical variables. The independent groups t test and the chi-square test was used, as appropriate, to analyze group differences.

Recruitment

Recruitment status

Completed

Date of first participant enrolment

Anticipated

2/08/2012

Actual

6/08/2012

Date of last participant enrolment

Anticipated

4/04/2013

Actual

25/04/2013

Date of last data collection

Anticipated

Actual

Sample size

Target

120

Accrual to date

Final

Recruitment outside Australia

Country [1]

Nigeria

State/province [1]

Oyo State / Ibadan

Funding & Sponsors

Funding source category [1]

Self funded/Unfunded

Name [1]

Address [1]

Country [1]

Primary sponsor type

Individual

Name

Dr. Emmanuel Achime

Address

Department of Obstetrics and Gynaecology, Faculty of Clinical Sciences, College of Medicine, University of Ibadan/University College Hospital, PMB 5116, Queen Elizabeth Road, Ibadan, Oyo State

Country

Nigeria

Secondary sponsor category [1]

None

Name [1]

Address [1]

Country [1]

Ethics approval

Ethics application status

Approved

Ethics committee name [1]

University of Ibadan/University College Hospital Ethical Review Committee

Ethics committee address [1]

Institute for Advanced Medical Research and Training (IAMRAT), College of Medicine, University of Ibadan/University College Hospital, PMB 5116, Queen Elizabeth Road, Orita Mefa, Ibadan, Oyo State,  Nigeria

Ethics committee country [1]

Nigeria

Date submitted for ethics approval [1]

Approval date [1]

17/07/2012

Ethics approval number [1]

UI/EC/12/0112 (UI/UCH/EC registration number: NHREC/05/01/2008a)

Summary

Brief summary

During antenatal visits, expectant mothers are routinely given information to educate them on what to expect during labour and delivery, in an effort to allay their fears. However most of this information is delivered verbally or with the aid of diagrammatic illustrations in an abstract manner. Previous studies in the United States of America (USA) have demonstrated the important role that online birth education plays on reducing anxiety. For example about 72 percent of women who were pregnant for the first time, and 34 percent of women who had been pregnant once before indicated their preference for audio-visual assistance prior to their delivery, in order to gain useful understanding of the process ahead. However, another study reported a different outcome, as 32 percent of first-time mothers felt more anxious after watching audiovisual displays about the birthing process. This may be due to the absence of quality control and screening of the contents in this study, thereby leading to a counterproductive and biased outcome of increasing anxiety, instead of diminishing it.  

The possible adverse effects of anxiety especially at such critical times in the life of an expectant mother and the unborn baby are immense, but unfortunately, ways to reduce these levels are yet to be explored. There are no studies among African women (including Nigeria) to show the effect of controlled use of audiovisuals on anxiety levels among mothers who have not experienced the childbirthing process. This study therefore aims to determine the effect of child birthing audiovisuals in the reduction of anxiety levels in first time mothers.

The general objective is to determine the influence of child birthing audiovisual on anxiety levels among pregnant women before, during and after childbirth, pain perception during labour and obstetric outcomes.
The specific objectives are: To determine the influence of audiovisuals of childbirth on anxiety levels among pregnant women before, during and after childbirth. And To determine the influence of antenatal audiovisuals on obstetric outcome for women in both arms of the study.

Material and Methods: The study was a randomized controlled trial among booked antenatal patients at the University College Hospital, Ibadan, Oyo State, Nigeria. Prospective mothers who met the criteria below were informed and recruited into the study.
The eligibility criteria included:
1.	Primigravid/ nulliparous pregnant women
2.	Anticipated vaginal delivery
3.	Absence of medical disorders (hypertension, Diabetes Mellitus)
4.	Singleton foetus in the current pregnancy
5.	28 -30 weeks gestation
The study was conducted at the University College Hospital, Ibadan (UCH), in south-west Nigeria from Octobert 2012 to June 2013. This health facility is an 850-bed hospital with an annual delivery rate of between 1500 and 2000. An average of 120 pregnant women are seen per week during antenatal care (ANC) clinic. At each antenatal clinic (ANC), the routine care involves registration, vital signs measurement and group health talk before consultation by doctors. The labour ward has an admission room, the first stage, delivery suite and theatre. 
Intervention: The intervention was a five minutes documentary film on the events that occur during the second stage of labour. This was shown to those in the experimental group after recruitment and assessment of baseline anxiety levels. Questions and clarifications were made during the course of the session to dispel misconceptions and improve knowledge among respondents in the experimental group.
Outcomes: The primary outcome was a significant change in level of anxiety in the treatment/intervention arm compared to the controls. The secondary outcome was a significant change in obstetric outcomes for those in the treatment arm compared to those in the control arm.

Trial website

Trial related presentations / publications

Public notes

Contacts

Principal investigator

Name

Dr Emmanuel Achime

Address

Department of Obstetrics and Gynaecology,
University College Hospital, PMB 5116, Queen Elizabeth Road,
Ibadan, Oyo State

Country

Nigeria

Phone

+234 803 474 3988

Fax

emmaachime @yahoo.com

Contact person for public queries

Name

Imran Morhason-Bello

Address

Department of Obstetrics and Gynaecology,
Faculty of Clinical Sciences,
College of Medicine,
University of Ibadan/University College Hospital,
PMB 5116, Queen Elizabeth Road, Ibadan, Oyo State

Country

Nigeria

Phone

+234 803 478 4402

Fax

onembello@yahoo.co.uk

Contact person for scientific queries

Name

Imran Morhason-Bello

Address

Department of Obstetrics and Gynaecology,
Faculty of Clinical Sciences,
College of Medicine,
University of Ibadan/University College Hospital,
PMB 5116, Queen Elizabeth Road, Ibadan, Oyo State

Country

Nigeria

Phone

+ 234 803 478 4402

Fax

onembello@yahoo.co.uk

No information has been provided regarding IPD availability

What supporting documents are/will be available?

No Supporting Document Provided

Results publications and other study-related documents

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