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A Mobile Mindfulness Programme for Individuals/Couples Experiencing Fertility Problems

MoMiFer-Study: Evaluation of a Mobile Mindfulness Program (mMP) in Individuals/Couples Experiencing Fertility Problems

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04143828
Acronym
MoMiFer
Enrollment
60
Registered
2019-10-29
Start date
2019-11-24
Completion date
2021-05-31
Last updated
2020-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Keywords

Infertility, Mobile Health, Mindfulness

Brief summary

Infertility and its treatment result in a considerate emotional burden and a recent guideline of the European Society of Human Reproduction (ESHRE) highlight the importance to support couples facing fertility problems. Mindfulness-based programs (MBPs) have been proven effective in improving well-being and combatting mood disturbances in a wide range of conditions in both treatment and prevention. The overall aim of this project is to evaluate the impact of a mobile mindfulness programme (mMP) on quality of life and emotional well-being in individuals/couples experiencing fertility problems. The present study is a two-group randomized controlled trial with assessments at baseline, at 1,5 months and at 3 months. Sixty couples experiencing fertility problems will be enrolled. They will be assigned to either an intervention group (immediate access to the mMP) or a control group (waitlist condition). The mobile MBP is developed by a team of experienced mindfulness trainers, clinical psychologists, and a psychiatrist and adheres to a standardized protocol. The primary outcomes will be quality of life and emotional distress. Secondary outcomes will be repetitive negative thinking, self-compassion and mindfulness skills. Additionally, the feasibility of the mMP will be evaluated.

Interventions

BEHAVIORALmobile mindfulness programme

The mobile mindfulness programme adheres to a standardized protocol developed from the MBSR curriculum (Kabat-Zinn, 1990). The program consists of six modules. Each module consists of a short movie (talking head) explaining the content and two audiofiles to guide experiential mindfulness meditation exercises. Participants can follow the different modules based on their own time-schedule. Key objectives are: (1) to increase awareness of one's present moment experience; (2) to teach an attitude of openness and acceptance (non-judging) toward one's experience.

Sponsors

Universitaire Ziekenhuizen KU Leuven
CollaboratorOTHER
KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants are randomly assigned to one of two conditions: The intervention group receives a mobile mindfulness programme (mMP). The participants in the control group are wait-listed. They will receive access to the mobile mindfulness programme after three months.

Eligibility

Sex/Gender
ALL
Age
18 Years to 43 Years
Healthy volunteers
No

Inclusion criteria

* Individuals/couples experiencing fertility problems (using the criteria for the definition of 'infertility', as in: the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse) (Zegers-Hochschild et al., 2017) * Both partners possess a smartphone * Both partners understand and speak Dutch * Written informed consent after been informed on all aspects of the study

Exclusion criteria

Not applicable

Design outcomes

Primary

MeasureTime frameDescription
Fertility related quality of lifeData collected at baseline (before randomisation), after 1.5 and 3 monthsChange in scores on the Fertility Quality of Life Questionnaire (FertiQol) - 24 items; scoring: 0-100 (the higher the better the quality of life)
emotional distressData collected at baseline (before randomisation), after 1.5 and 3 monthsChange in scores on experienced stress, anxiety and depression as measured by Experience Sampling Method (record emotions several times a day during 4 consecutive days); scoring with a sliding bar: 0-100 (the lower the less emotional distress)

Secondary

MeasureTime frameDescription
self-compassionData collected at baseline (before randomisation), after 1.5 and 3 monthsChange in scores on the Self Compassion Scale (SCS-NL-R) - 12 items; scoring: 12-60 (the higher the more self-compassion)
Emotional distressData collected at baseline (before randomisation), after 1,5 and 3 monthsChange in scores on the Depression, Anxiety and Stress Scale (DASS-21); scoring: 0-126 (the higher the more emotional distress)
repetitive negative thoughtsData collected at baseline (before randomisation), after 1.5 and 3 monthsChange in scores on the Perseverative Thinking Questionnaire (PTQ) - 15 items; scoring: 0-60 (the higher, the more repetitive negative thinking)
subjective quality of the mobile Mindfulness Programme (mMP)after 3 months in the intervention groupa shortened version of the subjective quality subscale of the Mobile App Rating Scale (MARS); scoring: 0-8 (the higher, the better the quality of the mMP)
use of the mobile Mindfulness Programme (mMP)After 1.5 and 3 months in the intervention groupevaluating the use of the mMP (frequency) in combination with a question on their motivation of (not) using mMP
Mindfulness skillsData collected at baseline (before randomisation), after 1,5 and 3 monthsChange in scores on the Comprehensive Inventory of Mindfulness Experiences (CHIME-SF) - 24 items; scoring: 24-144 (the higher the better the mindfulness skills)
mindfulness skillsData collected at baseline (before randomisation), after 1.5 and 3 monthsChange in scores on experienced mindfulness skills as measured by Experience Sampling Method (several times a day during 4 consecutive days); scoring with a sliding bar: 0-100 (the higher the better the mindfulness skills)

Countries

Belgium

Contacts

Primary ContactKatleen Van der Gucht, PhD
katleen.vandergucht@kuleuven.be+3216373183
Backup ContactTessy Boedt, MSc.
tessy.boedt@kuleuven.be+32486804604

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026