Massage as an Adjunct Approach to Care for Pregnant Women Who Have Experienced a Stillbirth

Sponsor
Fogarty Sarah (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05636553
Collaborator
Massage Therapy Foundation (Other), University of Western Sydney (Other)
75
1
20

Study Details

Study Description

Brief Summary

The goal of this mixed-methods single-arm study is to measure the feasibility of massage as an adjunct approach to care for pregnant women who have experienced a stillbirth. In order to provide pilot data, this intervention study will:

  1. Determine the feasibility and acceptability of the massage intervention and optimize the timing and outcome measures,

  2. Provide data for future use in an individual participant data systematic review, and

  3. Evaluate experiences of women undertaking the intervention

Participants will [ If there is a comparison group: Researchers will compare [insert groups] to see if [insert effects].

Condition or Disease Intervention/Treatment Phase
  • Other: Massage
N/A

Detailed Description

Research shows that women experiencing pregnancy after stillbirth experience anxiety, fear, and depression. There is a limited evidence of adjunct emotional care approaches for women to utilise to help manage pregnancy after a stillbirth. Massage may assist women who are pregnant after a stillbirth via decreasing anxiety, worry and stress.

Aim: To measure the feasibility of massage as an adjunct approach to care for pregnant women who have experienced a stillbirth.

Design: This study will use a convergent parallel mixed-methods, single arm repeated measures pilot trial design.

Setting: Massage therapists' private clinics across Australia. Participants: Subjects will include 75 pregnant women who have experienced a stillbirth in a previous pregnancy.

Intervention: Women will receive four massages within a four-month period at intervals of their choosing. The massage treatments are based on a vulnerability-to-stress concept which acknowledges the impact of stress on a pregnant woman based on a biopsychosocial model.

The massage protocol allows treatment to be individualised to meet the needs of the participant.

Main outcome measures: The primary outcomes are a) feasibility, b) acceptability and experience of the massage intervention and c) optimization - i.e., capacity of the outcome measures to capture the impact of the intervention received, and to determine when treatments are likely to be of most value.

Analysis Plan: Data will be analysed to meet the study objectives of determining feasibility, acceptability, optimising timing, and outcome measures, and to obtain preliminary data to understand the effects and value of massage on women who are pregnant after a stillbirth.

Significance of the work: Standard antenatal care is emotionally unsuitable for many women in pregnancies following a stillbirth and there is a lack of direct evidence on what interventions or approaches to care might benefit these women. Our proposed research will begin to address this lack of direct evidence.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
75 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
A convergent parallel mixed-methods, single arm repeated measures pilot trial designA convergent parallel mixed-methods, single arm repeated measures pilot trial design
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Mixed-methods Single-arm Study Evaluating the Feasibility of Massage as an Adjunct Approach to Care for Pregnant Women Who Have Experienced a Stillbirth
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Jan 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Massage

Women will receive four 60 minute massage consultations within a four-month period at intervals of their choosing.

Other: Massage
Individualised treatment using massage techniques such as longitudinal gliding, transverse gliding, digital ischemic pressure, transverse frictions, and transverse gliding.

Outcome Measures

Primary Outcome Measures

  1. To assess the feasibility of massage as an adjunct approach to care for pregnant women who have experienced a stillbirth as assessed using a mixed methods narrative and joint display approach [1 year]

    The quantitative and qualitative findings will be integrated using a narrative reporting approach and fit of data integration (coherence of the quantitative and qualitative findings) will be reported.

Secondary Outcome Measures

  1. Changes in worry from baseline to a week post treatment interventions using the self-reported Cambridge Worry Score [Through study completion, an average of 1 year]

  2. Changes in maternal anxiety symptoms from baseline to a week post treatment interventions using the Generalized Anxiety Disorder Assessment (GAD-7) [Through study completion, an average of 1 year]

  3. Changes in coping from baseline to a week post treatment interventions using the self-reported Revised Prenatal Coping Inventory [Through study completion, an average of 1 year]

  4. Changes in self-efficacy from baseline to a week post treatment interventions using the Strategies Used by People to Promote Health measure [Through study completion, an average of 1 year]

  5. Changes in maternal stress symptoms from baseline to a week post treatment interventions using the Perceived Stress Scale [Through study completion, an average of 1 year]

  6. Assessing empathy in the context of the therapeutic relationship via the Consultation and Relational Empathy patient-reported experience measure [Through study completion, an average of 1 year]

  7. Recruitment rates (proportion of people randomised/proportion of people eligible) [Through study completion, an average of 1 year]

  8. Retention rates (proportion of people providing the outcomes of interest/proportion randomised) [Through study completion, an average of 1 year]

  9. Compliance with completing the validated outcome measures (number of validated measures asked to complete/number of validated measures completed) [Through study completion, an average of 1 year]

  10. Elucidating participants' experience of massage in a pregnancy after a stillbirth using a qualitative in-depth interview [Through study completion, an average of 1 year]

    Thematic inductive analysis will be used to analyse the qualitative data

  11. Optimization of massage timing to determine when treatments are likely to be of most value presented as a average of time between treatments [Through study completion, an average of 1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant women 18 years of age or greater who have experienced a stillbirth (pregnancy loss from 20 weeks gestation) in a previous pregnancy.

  • Participants who had a medial termination from 20-weeks' gestation will be included in the study.

  • Participants must be able to attend one of the study pregnancy massage therapists' clinics located within Australia.

  • Having had previous massage experience is not an enrolment criterion, it is just not an exclusion criterion.

Exclusion Criteria:
  • Participants will be excluded if they are unable to receive the study treatments in the allocated time frame.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Fogarty Sarah
  • Massage Therapy Foundation
  • University of Western Sydney

Investigators

  • Principal Investigator: Sarah Fogarty, PhD, Western Sydney University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sarah Fogarty, Principal Investigator, Fogarty Sarah
ClinicalTrials.gov Identifier:
NCT05636553
Other Study ID Numbers:
  • 20705.66430
First Posted:
Dec 5, 2022
Last Update Posted:
Dec 5, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sarah Fogarty, Principal Investigator, Fogarty Sarah
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 5, 2022