Effect of Therapeutic Touch on Burnout and Well-Being in Midwives
Levels of Burnout and Well-Being Among Midwives: A Randomized Controlled Trial
1 other identifier
interventional
90
1 country
1
Brief Summary
This single-center, randomized controlled trial evaluates the effect of Therapeutic Touch on levels of burnout and psychological well-being among midwives who are actively working in a clinical setting. Participants are randomly allocated to one of three parallel groups: a Therapeutic Touch (intervention) group, a placebo/sham group, and a no-intervention control group. The investigators hypothesize that Therapeutic Touch will reduce burnout and improve psychological well-being compared with the placebo and control conditions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 2, 2026
CompletedStudy Start
First participant enrolled
July 2, 2026
CompletedFirst Posted
Study publicly available on registry
July 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 1, 2026
July 9, 2026
July 1, 2026
2 months
July 2, 2026
July 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in burnout level measured by the Maslach Burnout Inventory (MBI)
The Maslach Burnout Inventory is a 22-item, 5-point Likert scale with three subscales: emotional exhaustion (score range 0-36), depersonalization (0-20), and reduced personal accomplishment (0-32). Higher emotional exhaustion and depersonalization scores and lower personal accomplishment scores indicate greater burnout. Subscales are evaluated separately.
Baseline (pretest) and after the 4-week intervention (posttest)
Change in psychological well-being measured by the Psychological Well-Being Scale (PWB)
The Psychological Well-Being Scale (Diener flourishing short form) is an 8-item, 7-point Likert scale. Total scores range from 8 to 56, with higher scores indicating greater psychological resources and strengths.
Baseline (pretest) and after the 4-week intervention (posttest)
Study Arms (3)
Therapeutic Touch
EXPERIMENTALParticipants receive Therapeutic Touch, a non-invasive energy-field intervention, over a 4-week period.
Placebo / Sham
SHAM COMPARATORParticipants receive a sham/placebo procedure that mimics Therapeutic Touch without the intended energy-field component, over a 4-week period.
Control
NO INTERVENTIONParticipants receive no intervention and continue their usual routine.
Interventions
A non-invasive energy-field intervention in which the practitioner uses the hands to detect and rebalance imbalances in the participant's energy field, delivered over a 4-week period.
A placebo/sham procedure resembling Therapeutic Touch but without the intended energy-field component, delivered over a 4-week period.
Eligibility Criteria
You may qualify if:
- Aged 18-65 years
- Actively practicing midwifery in the field/clinic for at least one year
- No prior energy therapy (Reiki, healing touch, Therapeutic Touch)
- Literate and willing to volunteer for the study
- Open to communication and cooperation
You may not qualify if:
- Currently being followed for a psychiatric diagnosis
- Currently using antidepressant, anxiolytic, or sleep-regulating medication
- Having touch sensitivity or a phobia-level aversion to being touched
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Elazig Fethi Sekin City Hospital
Elâzığ, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aslihan Turan, PhD
KTO Karatay University
- SUB INVESTIGATOR
Busra Karaaslan
Elazıg Fethi Sekin Sehir Hastanesi
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Single-blind: the outcome assessor is blinded to group allocation.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 2, 2026
First Posted
July 9, 2026
Study Start
July 2, 2026
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
October 1, 2026
Last Updated
July 9, 2026
Record last verified: 2026-07