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Positive Adjustment Coping Intervention (PACI)

Primary Purpose

Infertility/Sterility

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Positive adjustment coping intervention
Brainteaser
Sponsored by
University Hospital Heidelberg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Infertility/Sterility focused on measuring assisted reproductive technology, embryo transfer, online intervention, rct

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

All couples undergoing infertility treatment (in vitro fertilization or intracytoplasmic sperm injection) at the Department of Gynecologic Endocrinology and Fertility Disorders at Heidelberg University Women's Hospital, which have

  • agreed to participate in the study
  • indicated their mobile phone number
  • sufficient knowledge of German language.

If one partner is refusing to participate, the other person may be admitted as an individual.

Exclusion Criteria:

  • denial of participation
  • non-existent smartphone
  • insufficient knowledge of German language

Sites / Locations

  • University Hospital Heidelberg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Positive adjustment coping intervention

Brainteaser

Arm Description

All persons allocated to the intervention group will receive daily text messages (SMS) to their smartphones with sentences for positive adjustment over two weeks starting from the day of the egg-cell punctuation.

All persons allocated to the comparison intervention group will receive daily text messages (SMS) to their smartphones with brainteasers over two weeks starting from the day of the egg-cell punctuation.

Outcomes

Primary Outcome Measures

Differences in the Screen IVF questionaire between the intervention groups
Differences in the ScreenIVF risk profile at post-measurement time between the intervention group of positive adjustment and the intervention comparison group with the brainteasers

Secondary Outcome Measures

Quantitative evaluation of participants' opinion about the intervention
Participants will be questioned about the perceived effectiveness and practicability of the intervention techniques with quantitative items (Rating scales).
Qualitative evaluation of participants' opinion about the intervention
Participants will be questioned about the recommendations to others concerning the intervention techniques (open questions)

Full Information

First Posted
March 29, 2017
Last Updated
September 26, 2019
Sponsor
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT03118219
Brief Title
Positive Adjustment Coping Intervention
Acronym
PACI
Official Title
Positive Adjustment in Case of Involuntary Childlessness - a Smartphone-supported Intervention Study as RCT
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
July 18, 2017 (Actual)
Primary Completion Date
June 12, 2019 (Actual)
Study Completion Date
August 8, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Involuntary childlessness is experienced as emotionally stressful, however psychosocial counseling is not always available on the spot. Aim of this RCT study is to examine the efficacy and acceptance of a psychological low-dose online intervention for couples in reproductive treatment.
Detailed Description
About 8% of all couples of reproductive age are involuntary childless, and just about 25,000 couples receive a medical treatment each year in Germany, which is experienced as "roller coaster of emotions". The positive effect of "face-to-face" counseling for couples with a desire for children has been proven. However, this does not yet apply to a variety of other forms of intervention, e.g. telephone or online counseling. In this study, the effectiveness of a smartphone-supported psychosocial intervention for women and men in reproductive treatment will be examined in a randomized controlled pre-post design. For this purpose, an intervention group and a comparison intervention group of each n = 60 couples in reproductive treatment will be examined at two points during a four-week interval using the ScreenIVF questionaire. The ScreenIVF will be completed paper-pencil before the intervention and online after the intervention. In the fourteen-day waiting period between oocyte puncture and pregnancy test (or the reappearance of menstruation), both groups receive either positive adjustment techniques or brainteasers.In addition, both groups are questioned one month after the post-measurement date on the perceived effectiveness and practicability of the intervention techniques. Sociodemographic variables (such as age, education) and medical data (such as diagnosis, previous treatment cycles) as potential moderators, as well as possible pregnancies at the second measurement time will be reported. No adverse effects or other risks are expected for the study participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility/Sterility
Keywords
assisted reproductive technology, embryo transfer, online intervention, rct

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
401 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Positive adjustment coping intervention
Arm Type
Experimental
Arm Description
All persons allocated to the intervention group will receive daily text messages (SMS) to their smartphones with sentences for positive adjustment over two weeks starting from the day of the egg-cell punctuation.
Arm Title
Brainteaser
Arm Type
Other
Arm Description
All persons allocated to the comparison intervention group will receive daily text messages (SMS) to their smartphones with brainteasers over two weeks starting from the day of the egg-cell punctuation.
Intervention Type
Other
Intervention Name(s)
Positive adjustment coping intervention
Intervention Description
see arm description
Intervention Type
Other
Intervention Name(s)
Brainteaser
Other Intervention Name(s)
Comparison intervention group
Intervention Description
see arm description
Primary Outcome Measure Information:
Title
Differences in the Screen IVF questionaire between the intervention groups
Description
Differences in the ScreenIVF risk profile at post-measurement time between the intervention group of positive adjustment and the intervention comparison group with the brainteasers
Time Frame
through study completion, an average of 2 years
Secondary Outcome Measure Information:
Title
Quantitative evaluation of participants' opinion about the intervention
Description
Participants will be questioned about the perceived effectiveness and practicability of the intervention techniques with quantitative items (Rating scales).
Time Frame
through study completion, an average of 2 years
Title
Qualitative evaluation of participants' opinion about the intervention
Description
Participants will be questioned about the recommendations to others concerning the intervention techniques (open questions)
Time Frame
through study completion, an average of 2 years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All couples undergoing infertility treatment (in vitro fertilization or intracytoplasmic sperm injection) at the Department of Gynecologic Endocrinology and Fertility Disorders at Heidelberg University Women's Hospital, which have agreed to participate in the study indicated their mobile phone number sufficient knowledge of German language. If one partner is refusing to participate, the other person may be admitted as an individual. Exclusion Criteria: denial of participation non-existent smartphone insufficient knowledge of German language
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tewes Wischmann, PD Dr.
Organizational Affiliation
University Hospital Heidelberg
Official's Role
Study Director
Facility Information:
Facility Name
University Hospital Heidelberg
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18628259
Citation
Lancastle D, Boivin J. A feasibility study of a brief coping intervention (PRCI) for the waiting period before a pregnancy test during fertility treatment. Hum Reprod. 2008 Oct;23(10):2299-307. doi: 10.1093/humrep/den257. Epub 2008 Jul 15.
Results Reference
background
PubMed Identifier
32779730
Citation
Palmer MJ, Henschke N, Villanueva G, Maayan N, Bergman H, Glenton C, Lewin S, Fonhus MS, Tamrat T, Mehl GL, Free C. Targeted client communication via mobile devices for improving sexual and reproductive health. Cochrane Database Syst Rev. 2020 Jul 14;8(8):CD013680. doi: 10.1002/14651858.CD013680.
Results Reference
derived
PubMed Identifier
31289056
Citation
Schick M, Roesner S, Germeyer A, Moessner M, Bauer S, Ditzen B, Wischmann T. Smartphone-supported Positive Adjustment Coping Intervention (PACI) for couples undergoing fertility treatment: a randomised controlled trial protocol. BMJ Open. 2019 Jul 9;9(7):e025288. doi: 10.1136/bmjopen-2018-025288.
Results Reference
derived
Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
https://www.klinikum.uni-heidelberg.de/personen/apl-prof-dr-sc-hum-tewes-wischmann-2809/
Available IPD/Information Comments
Study Data can be requested per mail to Tewes Wischmann

Learn more about this trial

Positive Adjustment Coping Intervention

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