Effects of Craniosacral Therapy in Primary Caregivers of Individuals With Special Needs

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-55
SponsorIstanbul Rumeli University

About this trial

This study aims to evaluate the effects of craniosacral therapy on pain, body awareness, depression, and quality of life in primary caregivers of individuals with special needs.

Primary caregivers often experience physical and psychological burden due to long-term caregiving responsibilities. Craniosacral therapy is a non-pharmacological, manual therapy approach that may help reduce pain, improve body awareness, and support overall well-being.

In this study, eligible primary caregivers will be assigned to either a craniosacral therapy group or a control group. The intervention group will receive craniosacral therapy sessions, while the control group will receive no therapeutic intervention during the study period. Outcome measures related to pain, body awareness, depression, and quality of life will be assessed before and after the intervention.

The results of this study may contribute to a better understanding of the potential benefits of craniosacral therapy for improving the physical and psychosocial health of primary caregivers of individuals with special needs.

Eligibility criteria

Qualifiers

Female gender

Being a primary caregiver of an individual with special needs

Aged between 18 and 55 years

Caring for an individual who has a valid Special Needs Assessment Report for Children (ÇÖZGER) or a Health Board Report for Adults (ESKR)

Disqualifiers

Pregnancy

Presence of a neurological condition (e.g., epilepsy, acute cerebrovascular event)

Presence of tumors or metastatic disease

Unwillingness to participate in the study

Trial design

Treatments tested in this trial

  • Craniosacral Therapy

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators